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id="toc-Available_forms-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Side_effects" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#Side_effects"> <div class="vector-toc-text"> 2 Side effects </div> </a> <ul id="toc-Side_effects-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Pharmacology" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#Pharmacology"> <div class="vector-toc-text"> 3 Pharmacology </div> </a> <button aria-controls="toc-Pharmacology-sublist" class="cdx-button cdx-button--weight-quiet cdx-button--icon-only vector-toc-toggle"> Toggle Pharmacology subsection </button> <ul id="toc-Pharmacology-sublist" class="vector-toc-list"> <li id="toc-Pharmacodynamics" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Pharmacodynamics"> <div class="vector-toc-text"> 3.1 Pharmacodynamics </div> </a> <ul id="toc-Pharmacodynamics-sublist" class="vector-toc-list"> <li id="toc-Progestogenic_and_off-target_activities" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Progestogenic_and_off-target_activities"> <div class="vector-toc-text"> 3.1.1 Progestogenic and off-target activities </div> </a> <ul id="toc-Progestogenic_and_off-target_activities-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Antigonadotropic_effects" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Antigonadotropic_effects"> <div class="vector-toc-text"> 3.1.2 Antigonadotropic effects </div> </a> <ul id="toc-Antigonadotropic_effects-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Other_activities" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Other_activities"> <div class="vector-toc-text"> 3.1.3 Other activities </div> </a> <ul id="toc-Other_activities-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Pharmacokinetics" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Pharmacokinetics"> <div class="vector-toc-text"> 3.2 Pharmacokinetics </div> </a> <ul id="toc-Pharmacokinetics-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Chemistry" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#Chemistry"> <div class="vector-toc-text"> 4 Chemistry </div> </a> <button aria-controls="toc-Chemistry-sublist" class="cdx-button cdx-button--weight-quiet cdx-button--icon-only vector-toc-toggle"> Toggle Chemistry subsection </button> <ul id="toc-Chemistry-sublist" class="vector-toc-list"> <li id="toc-Synthesis" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Synthesis"> <div class="vector-toc-text"> 4.1 Synthesis </div> </a> <ul id="toc-Synthesis-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li 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data-mw-ve-target-container> <div class="vector-body-before-content"> <div class="mw-indicators"> </div> <div id="siteSub" class="noprint">From Wikipedia, the free encyclopedia</div> </div> <div id="contentSub"><div id="mw-content-subtitle"></div></div> <div id="mw-content-text" class="mw-body-content"><div class="mw-content-ltr mw-parser-output" lang="en" dir="ltr"><div class="shortdescription nomobile noexcerpt noprint searchaux" style="display:none">Chemical compound</div> <style data-mw-deduplicate="TemplateStyles:r1257001546">.mw-parser-output .infobox-subbox{padding:0;border:none;margin:-3px;width:auto;min-width:100%;font-size:100%;clear:none;float:none;background-color:transparent}.mw-parser-output .infobox-3cols-child{margin:auto}.mw-parser-output .infobox .navbar{font-size:100%}@media screen{html.skin-theme-clientpref-night .mw-parser-output .infobox-full-data:not(.notheme)>div:not(.notheme)[style]{background:#1f1f23!important;color:#f8f9fa}}@media screen and (prefers-color-scheme:dark){html.skin-theme-clientpref-os .mw-parser-output .infobox-full-data:not(.notheme) div:not(.notheme){background:#1f1f23!important;color:#f8f9fa}}@media(min-width:640px){body.skin--responsive .mw-parser-output .infobox-table{display:table!important}body.skin--responsive .mw-parser-output .infobox-table>caption{display:table-caption!important}body.skin--responsive .mw-parser-output .infobox-table>tbody{display:table-row-group}body.skin--responsive .mw-parser-output .infobox-table tr{display:table-row!important}body.skin--responsive .mw-parser-output .infobox-table th,body.skin--responsive .mw-parser-output .infobox-table td{padding-left:inherit;padding-right:inherit}}</style><table class="infobox" style="border-spacing:2px;"><caption class="infobox-title">Allylestrenol</caption><tbody><tr><td colspan="2" class="infobox-image notheme" style="background-color: #f8f9fa;"><a href="/wiki/File:Allylestrenol.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a9/Allylestrenol.svg/200px-Allylestrenol.svg.png" decoding="async" width="200" height="179" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a9/Allylestrenol.svg/300px-Allylestrenol.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a9/Allylestrenol.svg/400px-Allylestrenol.svg.png 2x" data-file-width="512" data-file-height="457" /></a></td></tr><tr><td colspan="2" class="infobox-image notheme" style="background-color: #f8f9fa;"><a href="/wiki/File:Allylestrenol_molecule_ball.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/41/Allylestrenol_molecule_ball.png/250px-Allylestrenol_molecule_ball.png" decoding="async" width="250" height="175" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/41/Allylestrenol_molecule_ball.png/375px-Allylestrenol_molecule_ball.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/41/Allylestrenol_molecule_ball.png/500px-Allylestrenol_molecule_ball.png 2x" data-file-width="2560" data-file-height="1789" /></a></td></tr><tr><th colspan="2" class="infobox-header" style="background:#ddd">Clinical data</th></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Drug_nomenclature#Trade_names" title="Drug nomenclature">Trade names</a></th><td class="infobox-data">Gestanin, Gestanon, Perselin, Turinal, others</td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;">Other names</th><td class="infobox-data">Allyloestrenol; SC-6393; Org AL-25; 3-Deketo-17α-allyl-19-nortestosterone; 17α-Allylestr-4-en-17β-ol; 17α-(Prop-2-en-1-yl)estr-4-en-17β-ol</td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Pregnancy_category" title="Pregnancy category">Pregnancy category</a></th><td class="infobox-data"><style data-mw-deduplicate="TemplateStyles:r1126788409">.mw-parser-output .plainlist ol,.mw-parser-output .plainlist ul{line-height:inherit;list-style:none;margin:0;padding:0}.mw-parser-output .plainlist ol li,.mw-parser-output .plainlist ul li{margin-bottom:0}</style><div class="plainlist"> <ul><li>Used in threatened miscarriage and recurrent pregnancy loss</li></ul> </div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Route_of_administration" title="Route of administration">Routes of administration</a></th><td class="infobox-data"><a href="/wiki/Oral_administration" title="Oral administration">By mouth</a></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Drug_class" title="Drug class">Drug class</a></th><td class="infobox-data"><a href="/wiki/Progestogen_(medication)" title="Progestogen (medication)">Progestogen</a>; <a href="/wiki/Progestin" class="mw-redirect" title="Progestin">Progestin</a></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Anatomical_Therapeutic_Chemical_Classification_System" title="Anatomical Therapeutic Chemical Classification System">ATC code</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a href="/wiki/ATC_code_G03" title="ATC code G03">G03DC01</a> (<a rel="nofollow" class="external text" href="https://www.whocc.no/atc_ddd_index/?code=G03DC01">WHO</a>) </li></ul></div></td></tr><tr><th colspan="2" class="infobox-header" style="background:#ddd">Legal status</th></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Regulation_of_therapeutic_goods" title="Regulation of therapeutic goods">Legal status</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"> <ul><li>In general: ℞ (Prescription only)</li></ul></div> </td></tr><tr><th colspan="2" class="infobox-header" style="background:#ddd"><a href="/wiki/Pharmacokinetics" title="Pharmacokinetics">Pharmacokinetic</a> data</th></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Plasma_protein_binding" title="Plasma protein binding">Protein binding</a></th><td class="infobox-data">"Considerable"<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a> (and low affinity for <a href="/wiki/Sex_hormone-binding_globulin" title="Sex hormone-binding globulin"><abbr title="sex hormone-binding globulin">SHBG</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip sex hormone-binding globulin)<a href="#cite_note-BerginkLoonen1985-3">[3]</a></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Drug_metabolism" title="Drug metabolism">Metabolism</a></th><td class="infobox-data"><a href="/wiki/Liver" title="Liver">Liver</a> (<a href="/wiki/Redox" title="Redox">reduction</a>, <a href="/wiki/Hydroxylation" title="Hydroxylation">hydroxylation</a>, <a href="/wiki/Conjugation_(biochemistry)" class="mw-redirect" title="Conjugation (biochemistry)">conjugation</a>; <a href="/wiki/CYP3A4" title="CYP3A4">CYP3A4</a>)<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a><a href="#cite_note-SuperCYP-5">[5]</a></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Metabolite" title="Metabolite">Metabolites</a></th><td class="infobox-data">• <a href="/wiki/17%CE%B1-Allyl-19-nortestosterone" title="17α-Allyl-19-nortestosterone"><abbr title="17α-Allyl-19-nortestosterone">17α-Allyl-19-NT</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip 17α-Allyl-19-nortestosterone<a href="#cite_note-BerginkLoonen1985-3">[3]</a><a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Biological_half-life" title="Biological half-life">Elimination half-life</a></th><td class="infobox-data">"Several hours" or 10 hours<a href="#cite_note-SahaRoy2000-4">[4]</a><a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Excretion" title="Excretion">Excretion</a></th><td class="infobox-data"><a href="/wiki/Urine" title="Urine">Urine</a> (as conjugates)<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a></td></tr><tr><th colspan="2" class="infobox-header" style="background:#ddd">Identifiers</th></tr><tr><td colspan="2" class="infobox-full-data"><div class="collapsible-list mw-collapsible mw-collapsed" style="text-align: left;"> <div style="line-height: 1.6em; font-weight: bold;"><div><a href="/wiki/IUPAC_nomenclature_of_chemistry" title="IUPAC nomenclature of chemistry">IUPAC name</a></div></div> <ul class="mw-collapsible-content" style="margin-top: 0; margin-bottom: 0; line-height: inherit; list-style: none; margin-left: 0; word-break:break-all; text-align:left; padding-left:1.5em; text-indent:-1.5em;"><li style="line-height: inherit; margin: 0"><div style="font-size: 97%;">(8R,9S,10R,13S,14S,17R)-13-methyl-17-prop-2-enyl-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol</div></li></ul> </div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/CAS_Registry_Number" title="CAS Registry Number">CAS Number</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=432-60-0">432-60-0</a> <img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" />Y</li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/PubChem#CID" title="PubChem">PubChem</a> <abbr title="Compound ID">CID</abbr></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/235905">235905</a></li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/DrugBank" title="DrugBank">DrugBank</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://www.drugbank.ca/drugs/DB01431">DB01431</a> <img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" />Y</li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/ChemSpider" title="ChemSpider">ChemSpider</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://www.chemspider.com/Chemical-Structure.205855.html">205855</a> <img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" />Y</li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Unique_Ingredient_Identifier" title="Unique Ingredient Identifier">UNII</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://precision.fda.gov/uniisearch/srs/unii/I47VB5DZ8O">I47VB5DZ8O</a></li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/KEGG" title="KEGG">KEGG</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://www.kegg.jp/entry/D01374">D01374</a> <img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" />Y</li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/ChEBI" title="ChEBI">ChEBI</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:31189">CHEBI:31189</a> <img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" />Y</li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/ChEMBL" title="ChEMBL">ChEMBL</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://www.ebi.ac.uk/chembl/explore/compound/ChEMBL2105618">ChEMBL2105618</a> <img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" />Y</li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/CompTox_Chemicals_Dashboard" title="CompTox Chemicals Dashboard">CompTox Dashboard</a> (<abbr title="U.S. Environmental Protection Agency">EPA</abbr>)</th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://comptox.epa.gov/dashboard/chemical/details/DTXSID9022574">DTXSID9022574</a> <a href="https://www.wikidata.org/wiki/Q531965#P3117" title="Edit this at Wikidata"><img alt="Edit this at Wikidata" src="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png" decoding="async" width="10" height="10" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/15px-OOjs_UI_icon_edit-ltr-progressive.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/20px-OOjs_UI_icon_edit-ltr-progressive.svg.png 2x" data-file-width="20" data-file-height="20" /></a></li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/ECHA_InfoCard" class="mw-redirect" title="ECHA InfoCard">ECHA InfoCard</a></th><td class="infobox-data"><a rel="nofollow" class="external text" href="https://echa.europa.eu/substance-information/-/substanceinfo/100.006.440">100.006.440</a> <a href="https://www.wikidata.org/wiki/Q531965#P2566" title="Edit this at Wikidata"><img alt="Edit this at Wikidata" src="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png" decoding="async" width="10" height="10" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/15px-OOjs_UI_icon_edit-ltr-progressive.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/20px-OOjs_UI_icon_edit-ltr-progressive.svg.png 2x" data-file-width="20" data-file-height="20" /></a></td></tr><tr><th colspan="2" class="infobox-header" style="background:#ddd">Chemical and physical data</th></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Chemical_formula" title="Chemical formula">Formula</a></th><td class="infobox-data">C21H32O</td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Molar_mass" title="Molar mass">Molar mass</a></th><td class="infobox-data">300.486 g·mol−1</td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;">3D model (<a href="/wiki/JSmol" class="mw-redirect" title="JSmol">JSmol</a>)</th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><a rel="nofollow" class="external text" href="https://chemapps.stolaf.edu/jmol/jmol.php?model=C%5BC%40%5D12CC%5BC%40H%5D3%5BC%40H%5D%28%5BC%40%40H%5D1CC%5BC%40%5D2%28CC%3DC%29O%29CCC4%3DCCCC%5BC%40H%5D34">Interactive image</a></li></ul></div></td></tr><tr><td colspan="2" class="infobox-full-data"><div class="collapsible-list mw-collapsible mw-collapsed" style="text-align: left;"> <div style="line-height: 1.6em; font-weight: bold;"><div><a href="/wiki/Simplified_molecular-input_line-entry_system" class="mw-redirect" title="Simplified molecular-input line-entry system">SMILES</a></div></div> <ul class="mw-collapsible-content" style="margin-top: 0; margin-bottom: 0; line-height: inherit; list-style: none; margin-left: 0; word-break:break-all;"><li style="line-height: inherit; margin: 0"><div style="word-wrap:break-word; text-indent:-1.5em; text-align:left; padding-left:1.5em; font-size:97%; line-height:120%;">C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@]2(CC=C)O)CCC4=CCCC[C@H]34</div></li></ul> </div></td></tr><tr><td colspan="2" class="infobox-full-data"><div class="collapsible-list mw-collapsible mw-collapsed" style="text-align: left;"> <div style="line-height: 1.6em; font-weight: bold;"><div><a href="/wiki/International_Chemical_Identifier" title="International Chemical Identifier">InChI</a></div></div> <ul class="mw-collapsible-content" style="margin-top: 0; margin-bottom: 0; line-height: inherit; list-style: none; margin-left: 0; word-break:break-all;"><li style="line-height: inherit; margin: 0"><div style="word-wrap:break-word; text-indent:-1.5em; text-align:left; padding-left:1.5em; font-size:97%; line-height:120%;">InChI=1S/C21H32O/c1-3-12-21(22)14-11-19-18-9-8-15-6-4-5-7-16(15)17(18)10-13-20(19,21)2/h3,6,16-19,22H,1,4-5,7-14H2,2H3/t16-,17+,18+,19-,20-,21-/m0/s1 <img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" />Y</div></li><li style="line-height: inherit; margin: 0"><div style="word-wrap:break-word; text-indent:-1.5em; text-align:left; padding-left:1.5em; font-size:97%; line-height:120%;">Key:ATXHVCQZZJYMCF-XUDSTZEESA-N <img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" />Y</div></li></ul> </div></td></tr><tr><td colspan="2" class="infobox-below"><style data-mw-deduplicate="TemplateStyles:r886047488">.mw-parser-output .nobold{font-weight:normal}</style>  <a class="external text" href="https://en.wikipedia.org/w/index.php?title=Special:ComparePages&rev1=477248526&page2=Allylestrenol">(verify)</a></td></tr></tbody></table> Allylestrenol, sold under the brand names Gestanin and Turinal among others, is a <a href="/wiki/Progestin" class="mw-redirect" title="Progestin">progestin</a> medication which is used to treat <a href="/wiki/Habitual_abortion" class="mw-redirect" title="Habitual abortion">recurrent</a> and <a href="/wiki/Miscarriage" title="Miscarriage">threatened miscarriage</a> and to prevent <a href="/wiki/Premature_labor" class="mw-redirect" title="Premature labor">premature labor</a> in <a href="/wiki/Pregnancy" title="Pregnancy">pregnant</a> women.<a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-pmid7459930-7">[7]</a><a href="#cite_note-:0-8">[8]</a> However, except in the case of proven <a href="/wiki/Progesterone_deficiency" class="mw-redirect" title="Progesterone deficiency">progesterone deficiency</a>, its use for such purposes is no longer recommended.<a href="#cite_note-Martindale-6">[6]</a> It is also used in <a href="/wiki/Japan" title="Japan">Japan</a> to treat <a href="/wiki/Benign_prostatic_hyperplasia" title="Benign prostatic hyperplasia">benign prostatic hyperplasia</a> (BPH) in men.<a href="#cite_note-pmid1722627-9">[9]</a><a href="#cite_note-pmid1722628-10">[10]</a><a href="#cite_note-pmid12534901-11">[11]</a> The medication is used alone and is not formulated in combination with an <a href="/wiki/Estrogen_(medication)" title="Estrogen (medication)">estrogen</a>.<a href="#cite_note-Muller1998-12">[12]</a> It is taken <a href="/wiki/Oral_administration" title="Oral administration">by mouth</a>.<a href="#cite_note-Seth2009-13">[13]</a> <a href="/wiki/Side_effect" title="Side effect">Side effects</a> of allylestrenol are few and have not been well-defined, but are assumed to be similar to those of related medications.<a href="#cite_note-Borglin1960-14">[14]</a> Allylestrenol is a progestin, or a <a href="/wiki/Synthetic_compound" class="mw-redirect" title="Synthetic compound">synthetic</a> <a href="/wiki/Progestogen_(medication)" title="Progestogen (medication)">progestogen</a>, and hence is an <a href="/wiki/Agonist" title="Agonist">agonist</a> of the <a href="/wiki/Progesterone_receptor" title="Progesterone receptor">progesterone receptor</a>, the <a href="/wiki/Biological_target" title="Biological target">biological target</a> of progestogens like <a href="/wiki/Progesterone" title="Progesterone">progesterone</a>.<a href="#cite_note-pmid13699366-15">[15]</a> It has no other important <a href="/wiki/Hormonal_agent" class="mw-redirect" title="Hormonal agent">hormonal</a> activity.<a href="#cite_note-BerginkLoonen1985-3">[3]</a><a href="#cite_note-Madjerekde_Visser1960-16">[16]</a> The medication is a <a href="/wiki/Prodrug" title="Prodrug">prodrug</a> of <a href="/wiki/17%CE%B1-allyl-19-nortestosterone" class="mw-redirect" title="17α-allyl-19-nortestosterone">17α-allyl-19-nortestosterone</a> (3-ketoallylestrenol) in the body.<a href="#cite_note-pmid18395441-17">[17]</a><a href="#cite_note-Zeelen1990-18">[18]</a><a href="#cite_note-BerginkLoonen1985-3">[3]</a> Allylestrenol was first described in 1958 and was introduced for medical use by 1961.<a href="#cite_note-Publishing2013-19">[19]</a><a href="#cite_note-Field-RichardsSnaith1961-20">[20]</a><a href="#cite_note-SimpsonWeiner1997-21">[21]</a><a href="#cite_note-Juta1962-22">[22]</a> It has been marketed widely throughout the world in the past, but today its availability and usage are relatively limited.<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a> It remains available in a few <a href="/wiki/Europe" title="Europe">European</a> countries and in a number of <a href="/wiki/Asia" title="Asia">Asian</a> countries.<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a> <style data-mw-deduplicate="TemplateStyles:r886046785">.mw-parser-output .toclimit-2 .toclevel-1 ul,.mw-parser-output .toclimit-3 .toclevel-2 ul,.mw-parser-output .toclimit-4 .toclevel-3 ul,.mw-parser-output .toclimit-5 .toclevel-4 ul,.mw-parser-output .toclimit-6 .toclevel-5 ul,.mw-parser-output .toclimit-7 .toclevel-6 ul{display:none}</style><div class="toclimit-3"><meta property="mw:PageProp/toc" /></div> <div class="mw-heading mw-heading2"><h2 id="Medical_uses">Medical uses</h2>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=1" title="Edit section: Medical uses">edit</a>]</div> Allylestrenol is used in the treatment of <a href="/wiki/Habitual_abortion" class="mw-redirect" title="Habitual abortion">recurrent</a> and <a href="/wiki/Miscarriage" title="Miscarriage">threatened miscarriage</a> and to prevent <a href="/wiki/Premature_labor" class="mw-redirect" title="Premature labor">premature labor</a>.<a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-pmid7459930-7">[7]</a> However, except in the case of proven <a href="/wiki/Progesterone_deficiency" class="mw-redirect" title="Progesterone deficiency">progesterone deficiency</a>, its use for such indications is no longer recommended.<a href="#cite_note-Martindale-6">[6]</a> Allylestrenol is one of only a handful of progestogens that has commonly been used for such purposes, the others including <a href="/wiki/Progesterone_(medication)" title="Progesterone (medication)">progesterone</a>, <a href="/wiki/Hydroxyprogesterone_caproate" title="Hydroxyprogesterone caproate">hydroxyprogesterone caproate</a>, and <a href="/wiki/Dydrogesterone" title="Dydrogesterone">dydrogesterone</a>.<a href="#cite_note-:0-8">[8]</a> The medication has also been studied in the treatment of <a href="/wiki/Gynecological_disorder" class="mw-redirect" title="Gynecological disorder">gynecological disorders</a> such as <a href="/wiki/Amenorrhea" title="Amenorrhea">amenorrhea</a>, <a href="/wiki/Irregular_menstruation" title="Irregular menstruation">irregular menstruation</a>, and <a href="/wiki/Premenstrual_syndrome" title="Premenstrual syndrome">premenstrual syndrome</a>.<a href="#cite_note-Borglin1960-14">[14]</a> Unlike other progestins, allylestrenol has not been used in <a href="/wiki/Hormonal_contraception" title="Hormonal contraception">hormonal contraception</a> or in <a href="/wiki/Menopausal_hormone_therapy" class="mw-redirect" title="Menopausal hormone therapy">menopausal hormone therapy</a>. In one study, it was found to be inadequate for <a href="/wiki/Endometrial_transformation" class="mw-redirect" title="Endometrial transformation">endometrial transformation</a> in women in combination with <a href="/wiki/Estradiol_valerate" title="Estradiol valerate">estradiol valerate</a>.<a href="#cite_note-pmid3609436-26">[26]</a> On the other hand, allylestrenol was found to be effective in the treatment of <a href="/wiki/Hot_flash" title="Hot flash">hot flashes</a> in postmenopausal women.<a href="#cite_note-pmid1473164-27">[27]</a> Allylestrenol has been commonly used in <a href="/wiki/Japan" title="Japan">Japan</a> at high dosages, typically 50 mg/day but as much as 100 mg/day, to treat BPH in men.<a href="#cite_note-pmid12534901-11">[11]</a><a href="#cite_note-pmid6203385-28">[28]</a><a href="#cite_note-pmid2425610-29">[29]</a><a href="#cite_note-pmid2425611-30">[30]</a><a href="#cite_note-pmid2426932-31">[31]</a><a href="#cite_note-pmid2426933-32">[32]</a><a href="#cite_note-pmid2435122-33">[33]</a><a href="#cite_note-pmid1693037-34">[34]</a><a href="#cite_note-pmid1693038-35">[35]</a><a href="#cite_note-pmid1722627-9">[9]</a><a href="#cite_note-pmid1722628-10">[10]</a><a href="#cite_note-pmid1384295-36">[36]</a><a href="#cite_note-pmid7689782-37">[37]</a><a href="#cite_note-pmid7513937-38">[38]</a><a href="#cite_note-pmid7541089-39">[39]</a><a href="#cite_note-pmid9781436-40">[40]</a><a href="#cite_note-pmid11107528-41">[41]</a><a href="#cite_note-pmid12094708-42">[42]</a><a href="#cite_note-pmid16910584-43">[43]</a> Related medications that have similarly been used to treat BPH, particularly in Japan, include <a href="/wiki/Chlormadinone_acetate" title="Chlormadinone acetate">chlormadinone acetate</a>, <a href="/wiki/Gestonorone_caproate" title="Gestonorone caproate">gestonorone caproate</a>, and <a href="/wiki/Oxendolone" title="Oxendolone">oxendolone</a>.<a href="#cite_note-pmid2435122-33">[33]</a><a href="#cite_note-pmid7513937-38">[38]</a> Allylestrenol has also been studied in the treatment of <a href="/wiki/Prostate_cancer" title="Prostate cancer">prostate cancer</a> in Japan.<a href="#cite_note-pmid6281750-44">[44]</a><a href="#cite_note-pmid6203385-28">[28]</a> The medication has been studied as a <a href="/wiki/Puberty_blocker" title="Puberty blocker">puberty blocker</a> in the treatment of <a href="/wiki/Precocious_puberty" title="Precocious puberty">precocious puberty</a> as well.<a href="#cite_note-pmid5057420-45">[45]</a> <div class="mw-heading mw-heading3"><h3 id="Available_forms">Available forms</h3>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=2" title="Edit section: Available forms">edit</a>]</div> Allylestrenol is available in the form of 5 mg <a href="/wiki/Oral_administration" title="Oral administration">oral</a> <a href="/wiki/Tablet_(pharmacy)" title="Tablet (pharmacy)">tablets</a>.<a href="#cite_note-Muller1998-12">[12]</a><a href="#cite_note-Tripathi2013-46">[46]</a><a href="#cite_note-SatoskarRege1973-47">[47]</a> It is typically used at a dosage of 5 to 40 mg/day.<a href="#cite_note-Tripathi2013-46">[46]</a><a href="#cite_note-SatoskarRege1973-47">[47]</a> In <a href="/wiki/Japan" title="Japan">Japan</a>, a 25 mg allylestrenol oral tablet, under the brand name Perselin, is marketed for the treatment of BPH.<a href="#cite_note-pmid7689782-37">[37]</a> <div class="mw-heading mw-heading2"><h2 id="Side_effects">Side effects</h2>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=3" title="Edit section: Side effects">edit</a>]</div> <style data-mw-deduplicate="TemplateStyles:r1236090951">.mw-parser-output .hatnote{font-style:italic}.mw-parser-output div.hatnote{padding-left:1.6em;margin-bottom:0.5em}.mw-parser-output .hatnote i{font-style:normal}.mw-parser-output .hatnote+link+.hatnote{margin-top:-0.5em}@media print{body.ns-0 .mw-parser-output .hatnote{display:none!important}}</style><div role="note" class="hatnote navigation-not-searchable">See also: <a href="/wiki/Progestin#Side_effects" class="mw-redirect" title="Progestin">Progestin § Side effects</a></div> Allylestrenol should not be taken by people who are allergic to <a href="/wiki/Ibuprofen" title="Ibuprofen">ibuprofen</a> or <a href="/wiki/Naproxen" title="Naproxen">naproxen</a>,<a href="#cite_note-:1-48">[48]</a> or who have <a href="/wiki/Salicylate_intolerance" class="mw-redirect" title="Salicylate intolerance">salicylate intolerance</a><a href="#cite_note-49">[49]</a> or a more generalized <a href="/wiki/Drug_intolerance" title="Drug intolerance">drug intolerance</a> to NSAIDs, and caution should be exercised in those with <a href="/wiki/Asthma" title="Asthma">asthma</a> or NSAID-precipitated <a href="/wiki/Bronchospasm" title="Bronchospasm">bronchospasm</a>. Owing to its effect on the stomach lining, manufacturers recommend people with <a href="/wiki/Peptic_ulcer" class="mw-redirect" title="Peptic ulcer">peptic ulcers</a>, mild <a href="/wiki/Diabetes" title="Diabetes">diabetes</a>, or <a href="/wiki/Gastritis" title="Gastritis">gastritis</a> seek medical advice before using allylestrenol.<a href="#cite_note-:1-48">[48]</a> <a href="/wiki/Side_effect" title="Side effect">Side effects</a> of allylestrenol are few and have not been well-defined, but are assumed to be similar to those of related medications (i.e., other progestins).<a href="#cite_note-Borglin1960-14">[14]</a> When used at high dosages in the treatment of BPH in men, allylestrenol can cause <a href="/wiki/Symptom" class="mw-redirect" title="Symptom">symptoms</a> of <a href="/wiki/Hypogonadism" title="Hypogonadism">hypogonadism</a> and <a href="/wiki/Sexual_dysfunction" title="Sexual dysfunction">sexual dysfunction</a>.<a href="#cite_note-pmid2426932-31">[31]</a><a href="#cite_note-pmid1693037-34">[34]</a><a href="#cite_note-pmid1693038-35">[35]</a> The medication <a href="/wiki/Indeloxazine" title="Indeloxazine">indeloxazine</a> may be able to counteract allylestrenol-associated sexual dysfunction.<a href="#cite_note-pmid7541089-39">[39]</a> Allylestrenol has no <a href="/wiki/Androgen" title="Androgen">androgenic</a> or other <a href="/wiki/Off-target_activity" title="Off-target activity">off-target</a> <a href="/wiki/Hormone" title="Hormone">hormonal</a> side effects.<a href="#cite_note-pmid2426932-31">[31]</a><a href="#cite_note-BerginkLoonen1985-3">[3]</a><a href="#cite_note-Madjerekde_Visser1960-16">[16]</a> <div class="mw-heading mw-heading2"><h2 id="Pharmacology">Pharmacology</h2>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=4" title="Edit section: Pharmacology">edit</a>]</div> <div class="mw-heading mw-heading3"><h3 id="Pharmacodynamics">Pharmacodynamics</h3>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=5" title="Edit section: Pharmacodynamics">edit</a>]</div> <figure class="mw-halign-right" typeof="mw:File/Thumb"><a href="/wiki/File:17%CE%B1-Allyl-19-nortestosterone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/29/17%CE%B1-Allyl-19-nortestosterone.svg/225px-17%CE%B1-Allyl-19-nortestosterone.svg.png" decoding="async" width="225" height="177" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/29/17%CE%B1-Allyl-19-nortestosterone.svg/338px-17%CE%B1-Allyl-19-nortestosterone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/29/17%CE%B1-Allyl-19-nortestosterone.svg/450px-17%CE%B1-Allyl-19-nortestosterone.svg.png 2x" data-file-width="1125" data-file-height="885" /></a><figcaption><a href="/wiki/17%CE%B1-Allyl-19-nortestosterone" title="17α-Allyl-19-nortestosterone">17α-Allyl-19-nortestosterone</a>, also known as 3-ketoallylestrenol, the <a href="/wiki/Active_metabolite" title="Active metabolite">active form</a> of allylestrenol.</figcaption></figure> <div class="mw-heading mw-heading4"><h4 id="Progestogenic_and_off-target_activities">Progestogenic and off-target activities</h4>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=6" title="Edit section: Progestogenic and off-target activities">edit</a>]</div> Allylestrenol is a <a href="/wiki/Progestogen_(medication)" title="Progestogen (medication)">progestogen</a>, or an <a href="/wiki/Agonist" title="Agonist">agonist</a> of the <a href="/wiki/Progesterone_receptor" title="Progesterone receptor">progesterone receptor</a> (PR).<a href="#cite_note-pmid13699366-15">[15]</a> It is lacking the <a href="/wiki/Keto_group" class="mw-redirect" title="Keto group">keto group</a> at the C3 position (part of the important 3-keto-4-ene structure) that is common in progestogens and is considered to be necessary for activity, and in relation to this, is thought to be a <a href="/wiki/Prodrug" title="Prodrug">prodrug</a> of <a href="/wiki/17%CE%B1-allyl-19-nortestosterone" class="mw-redirect" title="17α-allyl-19-nortestosterone">17α-allyl-19-nortestosterone</a> (3-ketoallylestrenol).<a href="#cite_note-pmid18395441-17">[17]</a><a href="#cite_note-Zeelen1990-18">[18]</a><a href="#cite_note-pmid7065053-50">[50]</a> Allylestrenol is a far less potent progestogen than many other 19-nortestosterone derivatives.<a href="#cite_note-pmid13699366-15">[15]</a> The effective <a href="/wiki/Ovulation" title="Ovulation">ovulation</a>-inhibiting or <a href="/wiki/Contraceptive" class="mw-redirect" title="Contraceptive">contraceptive</a> dosage of allylestrenol in women has been studied, albeit limitedly.<a href="#cite_note-pmid22078182-51">[51]</a> At 20 mg/day allylestrenol, ovulation occurred in 50% of 6 cycles, and at 25 mg/day, ovulation occurred in 0% of 3 cycles.<a href="#cite_note-pmid22078182-51">[51]</a><a href="#cite_note-Pincus2013-52">[52]</a> The total <a href="/wiki/Endometrial_transformation" class="mw-redirect" title="Endometrial transformation">endometrial transformation</a> dosage of allylestrenol in women across the cycle is 150 to 250 mg.<a href="#cite_note-LeidenbergerStrowitzki2009-53">[53]</a> Unlike virtually all other 19-nortestosterone derivatives, allylestrenol is reported to be a pure progestogen and hence to be devoid of <a href="/wiki/Androgen" title="Androgen">androgenic</a>, <a href="/wiki/Estrogen_(medication)" title="Estrogen (medication)">estrogenic</a>, and <a href="/wiki/Glucocorticoid" title="Glucocorticoid">glucocorticoid</a> activity.<a href="#cite_note-BerginkLoonen1985-3">[3]</a><a href="#cite_note-Madjerekde_Visser1960-16">[16]</a> As such, it appears to have properties more similar to those of natural <a href="/wiki/Progesterone_(medication)" title="Progesterone (medication)">progesterone</a>.<a href="#cite_note-BerginkLoonen1985-3">[3]</a><a href="#cite_note-Madjerekde_Visser1960-16">[16]</a> The binding and activity profiles of allylestrenol and its major <a href="/wiki/Active_metabolite" title="Active metabolite">active metabolite</a> at <a href="/wiki/Steroid_hormone_receptor" title="Steroid hormone receptor">steroid hormone receptors</a> and related <a href="/wiki/Protein" title="Protein">proteins</a> have been studied.<a href="#cite_note-BerginkLoonen1985-3">[3]</a><a href="#cite_note-pmid18395441-17">[17]</a> Allylestrenol has less than 0.2% of the <a href="/wiki/Affinity_(pharmacology)" class="mw-redirect" title="Affinity (pharmacology)">affinity</a> of <a href="/wiki/ORG-2058" title="ORG-2058">ORG-2058</a> and less than 2% of the affinity of progesterone for the PR.<a href="#cite_note-BerginkLoonen1985-3">[3]</a> Similarly, it has less than 0.2% of the affinity of <a href="/wiki/Testosterone_(medication)" title="Testosterone (medication)">testosterone</a> for the <a href="/wiki/Androgen_receptor" title="Androgen receptor">androgen receptor</a> (AR), less than 0.2% of the affinity of <a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">estradiol</a> for the <a href="/wiki/Estrogen_receptor" title="Estrogen receptor">estrogen receptor</a> (ER), less than 0.2% of the affinity of <a href="/wiki/Dexamethasone" title="Dexamethasone">dexamethasone</a> for the <a href="/wiki/Glucocorticoid_receptor" title="Glucocorticoid receptor">glucocorticoid receptor</a> (GR), and 0.9% of the affinity of testosterone for <a href="/wiki/Sex_hormone-binding_globulin" title="Sex hormone-binding globulin">sex hormone-binding globulin</a> (SHBG).<a href="#cite_note-BerginkLoonen1985-3">[3]</a> Conversely, its <a href="/wiki/Metabolite" title="Metabolite">metabolite</a> 17α-allyl-19-nortestosterone has 24% of the affinity of ORG-2058 and 186% of the affinity of progesterone for the PR, 4.5% of the affinity of testosterone for the AR, 9.8% of the affinity of dexamethasone for the GR, and 2.8% of the affinity of testosterone for SHBG, while it similarly has less than 0.2% of the affinity of estradiol for the ER.<a href="#cite_note-BerginkLoonen1985-3">[3]</a> The affinity of 17α-allyl-19-nortestosterone for the AR was less than that of <a href="/wiki/Norethisterone" title="Norethisterone">norethisterone</a> and <a href="/wiki/Medroxyprogesterone_acetate" title="Medroxyprogesterone acetate">medroxyprogesterone acetate</a> and its affinity for SHBG was much lower than that of norethisterone.<a href="#cite_note-BerginkLoonen1985-3">[3]</a> These findings may help to explain the absence of <a href="/wiki/Teratogen" class="mw-redirect" title="Teratogen">teratogenic</a> effects of allylestrenol on the <a href="/wiki/External_genitalia" class="mw-redirect" title="External genitalia">external genitalia</a> of female and male rat <a href="/wiki/Fetus" title="Fetus">fetuses</a>.<a href="#cite_note-BerginkLoonen1985-3">[3]</a> <table class="wikitable mw-collapsible mw-collapsed" style="text-align:left; margin-left:auto; margin-right:auto; border:none;"> <caption class="nowrap">Relative affinities (%) of allylestrenol and metabolites </caption> <tbody><tr> <th>Compound</th> <th><a href="/wiki/Progesterone_receptor" title="Progesterone receptor"><abbr title="Progesterone receptor">PR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Progesterone receptor</th> <th><a href="/wiki/Androgen_receptor" title="Androgen receptor"><abbr title="Androgen receptor">AR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Androgen receptor</th> <th><a href="/wiki/Estrogen_receptor" title="Estrogen receptor"><abbr title="Estrogen receptor">ER</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Estrogen receptor</th> <th><a href="/wiki/Glucocorticoid_receptor" title="Glucocorticoid receptor"><abbr title="Glucocorticoid receptor">GR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Glucocorticoid receptor</th> <th><a href="/wiki/Mineralocorticoid_receptor" title="Mineralocorticoid receptor"><abbr title="Mineralocorticoid receptor">MR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Mineralocorticoid receptor</th> <th><a href="/wiki/Sex_hormone-binding_globulin" title="Sex hormone-binding globulin"><abbr title="Sex hormone-binding globulin">SHBG</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Sex hormone-binding globulin</th> <th><a href="/wiki/Corticosteroid_binding_globulin" class="mw-redirect" title="Corticosteroid binding globulin"><abbr title="Corticosteroid binding globulin">CBG</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Corticosteroid binding globulin </th></tr> <tr> <td>Allylestrenol</td> <td>0</td> <td>0</td> <td>0</td> <td>0</td> <td>?</td> <td>1</td> <td>? </td></tr> <tr> <td><a href="/wiki/17%CE%B1-Allyl-19-nortestosterone" title="17α-Allyl-19-nortestosterone"><abbr title="17α-Allyl-19-nortestosterone">17α-Allyl-19-NT</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip 17α-Allyl-19-nortestosterone</td> <td>186</td> <td>5</td> <td>0</td> <td>10</td> <td>?</td> <td>3</td> <td>? </td></tr> <tr class="sortbottom"> <td colspan="8" style="width: 1px; background-color:#eaecf0; text-align: center;">Notes: Values are percentages (%). Reference <a href="/wiki/Ligand_(biochemistry)" title="Ligand (biochemistry)">ligands</a> (100%) were <a href="/wiki/Progesterone_(medication)" title="Progesterone (medication)"><abbr title="progesterone (medication)">P4</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip progesterone (medication) for the <a href="/wiki/Progesterone_receptor" title="Progesterone receptor"><abbr title="progesterone receptor">PR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip progesterone receptor, <a href="/wiki/Testosterone_(medication)" title="Testosterone (medication)"><abbr title="testosterone (medication)">T</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip testosterone (medication) for the <a href="/wiki/Androgen_receptor" title="Androgen receptor"><abbr title="androgen receptor">AR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip androgen receptor, <a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)"><abbr title="estradiol">E2</abbr></a> for the <a href="/wiki/Estrogen_receptor" title="Estrogen receptor"><abbr title="estrogen receptor">ER</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip estrogen receptor, <a href="/wiki/Dexamethasone" title="Dexamethasone"><abbr title="dexamethasone">DEXA</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip dexamethasone for the <a href="/wiki/Glucocorticoid_receptor" title="Glucocorticoid receptor"><abbr title="glucocorticoid receptor">GR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip glucocorticoid receptor, <a href="/wiki/Aldosterone" title="Aldosterone">aldosterone</a> for the <a href="/wiki/Mineralocorticoid_receptor" title="Mineralocorticoid receptor"><abbr title="mineralocorticoid receptor">MR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip mineralocorticoid receptor, <a href="/wiki/Testosterone_(medication)" title="Testosterone (medication)"><abbr title="testosterone (medication)">T</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip testosterone (medication) for <a href="/wiki/Sex_hormone-binding_globulin" title="Sex hormone-binding globulin"><abbr title="sex hormone-binding globulin">SHBG</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip sex hormone-binding globulin, and <a href="/wiki/Hydrocortisone" title="Hydrocortisone">cortisol</a> for <a href="/wiki/Corticosteroid-binding_globulin" class="mw-redirect" title="Corticosteroid-binding globulin"><abbr title="Corticosteroid-binding globulin">CBG</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Corticosteroid-binding globulin. Sources: <a href="#cite_note-BerginkLoonen1985-3">[3]</a> </td></tr></tbody></table> <div class="mw-heading mw-heading4"><h4 id="Antigonadotropic_effects">Antigonadotropic effects</h4>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=7" title="Edit section: Antigonadotropic effects">edit</a>]</div> <figure class="mw-halign-right" typeof="mw:File/Thumb"><a href="/wiki/File:Testosterone_levels_with_50_mg_per_day_allylestrenol_or_50_mg_per_day_chlormadinone_acetate_over_12_weeks_in_men_with_benign_prostatic_hyperplasia.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e5/Testosterone_levels_with_50_mg_per_day_allylestrenol_or_50_mg_per_day_chlormadinone_acetate_over_12_weeks_in_men_with_benign_prostatic_hyperplasia.png/300px-Testosterone_levels_with_50_mg_per_day_allylestrenol_or_50_mg_per_day_chlormadinone_acetate_over_12_weeks_in_men_with_benign_prostatic_hyperplasia.png" decoding="async" width="300" height="271" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e5/Testosterone_levels_with_50_mg_per_day_allylestrenol_or_50_mg_per_day_chlormadinone_acetate_over_12_weeks_in_men_with_benign_prostatic_hyperplasia.png/450px-Testosterone_levels_with_50_mg_per_day_allylestrenol_or_50_mg_per_day_chlormadinone_acetate_over_12_weeks_in_men_with_benign_prostatic_hyperplasia.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e5/Testosterone_levels_with_50_mg_per_day_allylestrenol_or_50_mg_per_day_chlormadinone_acetate_over_12_weeks_in_men_with_benign_prostatic_hyperplasia.png/600px-Testosterone_levels_with_50_mg_per_day_allylestrenol_or_50_mg_per_day_chlormadinone_acetate_over_12_weeks_in_men_with_benign_prostatic_hyperplasia.png 2x" data-file-width="1275" data-file-height="1150" /></a><figcaption><a href="/wiki/Testosterone" title="Testosterone">Testosterone</a> levels with 50 mg/day allylestrenol or 50 mg/day <a href="/wiki/Chlormadinone_acetate" title="Chlormadinone acetate">chlormadinone acetate</a> orally over 12 weeks in men with <a href="/wiki/Benign_prostatic_hyperplasia" title="Benign prostatic hyperplasia">benign prostatic hyperplasia</a>.<a href="#cite_note-pmid1693037-34">[34]</a></figcaption></figure> Similarly to other progestogens, allylestrenol has potent <a href="/wiki/Antigonadotropic" class="mw-redirect" title="Antigonadotropic">antigonadotropic</a> effects.<a href="#cite_note-pmid9268084-54">[54]</a> It is able to considerably decrease circulating concentrations of <a href="/wiki/Luteinizing_hormone" title="Luteinizing hormone">luteinizing hormone</a>, <a href="/wiki/Testosterone" title="Testosterone">testosterone</a>, and <a href="/wiki/Dihydrotestosterone" title="Dihydrotestosterone">dihydrotestosterone</a> in men.<a href="#cite_note-pmid2426933-32">[32]</a><a href="#cite_note-pmid1693037-34">[34]</a><a href="#cite_note-pmid7541089-39">[39]</a><a href="#cite_note-pmid9781436-40">[40]</a> At a dosage of 50 mg/day, allylestrenol has been found to suppress circulating testosterone levels by 78% in men with BPH.<a href="#cite_note-pmid9268084-54">[54]</a> This is about the maximum that progestogens are known to be able to suppress testosterone levels in men.<a href="#cite_note-pmid7000222-55">[55]</a><a href="#cite_note-pmid6237116-56">[56]</a><a href="#cite_note-pmid694436-57">[57]</a> In accordance, the reduction of testosterone and luteinizing hormone levels with allylestrenol in men has been found in a study to be equivalent to that of <a href="/wiki/Chlormadinone_acetate" title="Chlormadinone acetate">chlormadinone acetate</a> and <a href="/wiki/Oxendolone" title="Oxendolone">oxendolone</a>.<a href="#cite_note-pmid2435122-33">[33]</a> However, another study found a significantly lower decrease in testosterone levels with 50 mg/day allylestrenol relative to 50 mg/day chlormadinone acetate of about 49–52% versus 76–85%, respectively.<a href="#cite_note-pmid1693037-34">[34]</a> <a href="/wiki/Animal_research" class="mw-redirect" title="Animal research">Animal research</a> suggests that allylestrenol produces its beneficial effects in BPH via its antigonadotropic effects and consequent suppression of <a href="/wiki/Androgen" title="Androgen">androgen</a> levels and inhibition of <a href="/wiki/Prostate_gland" class="mw-redirect" title="Prostate gland">prostate gland</a> <a href="/wiki/Cell_growth" title="Cell growth">growth</a>, similarly to other progestins.<a href="#cite_note-pmid9268084-54">[54]</a> Some studies have found that allylestrenol is less effective for BPH than chlormadinone acetate but also produces fewer <a href="/wiki/Side_effect" title="Side effect">side effects</a> and <a href="/wiki/Sexual_dysfunction" title="Sexual dysfunction">sexual dysfunction</a>.<a href="#cite_note-pmid2426932-31">[31]</a><a href="#cite_note-pmid1693037-34">[34]</a><a href="#cite_note-pmid1693038-35">[35]</a> Allylestrenol therapy for BPH is associated with a significant decrease in <a href="/wiki/Prostate-specific_antigen" title="Prostate-specific antigen">prostate-specific antigen</a> levels, which may mask the detection of prostate cancer.<a href="#cite_note-pmid9268084-54">[54]</a><a href="#cite_note-pmid16910584-43">[43]</a> <div class="mw-heading mw-heading4"><h4 id="Other_activities">Other activities</h4>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=8" title="Edit section: Other activities">edit</a>]</div> Allylestrenol is not a significant <a href="/wiki/5%CE%B1-reductase_inhibitor" class="mw-redirect" title="5α-reductase inhibitor">5α-reductase inhibitor</a>.<a href="#cite_note-pmid9268084-54">[54]</a> In one study, it showed about 80,000-fold lower <a href="/wiki/Potency_(pharmacology)" title="Potency (pharmacology)">potency</a> for <a href="/wiki/Enzyme_inhibition" class="mw-redirect" title="Enzyme inhibition">inhibition</a> of <a href="/wiki/5%CE%B1-reductase" class="mw-redirect" title="5α-reductase">5α-reductase</a> <a href="/wiki/In_vitro" title="In vitro">in vitro</a> than the established 5α-reductase inhibitor <a href="/wiki/Epristeride" title="Epristeride">epristeride</a> (<a href="/wiki/Half-maximal_inhibitory_concentration" class="mw-redirect" title="Half-maximal inhibitory concentration"><abbr title="half-maximal inhibitory concentration">IC50</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip half-maximal inhibitory concentration = 11.3 nM for epristeride and 890 μM for allylestrenol).<a href="#cite_note-pmid9268084-54">[54]</a> In another study, there was 70% inhibition of 5α-reductase by allylestrenol at a concentration of 60 μM.<a href="#cite_note-pmid9268084-54">[54]</a> This difference may have been due to different experimental conditions, but is still much lower than epristeride.<a href="#cite_note-pmid9268084-54">[54]</a> <div class="mw-heading mw-heading3"><h3 id="Pharmacokinetics">Pharmacokinetics</h3>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=9" title="Edit section: Pharmacokinetics">edit</a>]</div> Following <a href="/wiki/Oral_administration" title="Oral administration">oral administration</a>, <a href="/wiki/Cmax_(pharmacology)" title="Cmax (pharmacology)">peak levels</a> of allylestrenol occur after 2 to 4 hours.<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a> The medication shows considerable <a href="/wiki/Plasma_protein_binding" title="Plasma protein binding">plasma protein binding</a>.<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a> It has relatively low affinity for SHBG, much lower than that of norethisterone.<a href="#cite_note-BerginkLoonen1985-3">[3]</a> Allylestrenol is <a href="/wiki/Metabolism" title="Metabolism">metabolized</a> in the <a href="/wiki/Liver" title="Liver">liver</a>, via <a href="/wiki/Redox" title="Redox">reduction</a>, <a href="/wiki/Hydroxylation" title="Hydroxylation">hydroxylation</a>, and <a href="/wiki/Conjugation_(biochemistry)" class="mw-redirect" title="Conjugation (biochemistry)">conjugation</a>.<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a> It is known to be a <a href="/wiki/Substrate_(biochemistry)" class="mw-redirect" title="Substrate (biochemistry)">substrate</a> of <a href="/wiki/CYP3A4" title="CYP3A4">CYP3A4</a>.<a href="#cite_note-SuperCYP-5">[5]</a> It is thought to be a <a href="/wiki/Prodrug" title="Prodrug">prodrug</a> of <a href="/wiki/17%CE%B1-allyl-19-nortestosterone" class="mw-redirect" title="17α-allyl-19-nortestosterone">17α-allyl-19-nortestosterone</a> (3-ketoallylestrenol), which, in accordance, is a known <a href="/wiki/Active_metabolite" title="Active metabolite">active metabolite</a> of allylestrenol.<a href="#cite_note-pmid18395441-17">[17]</a><a href="#cite_note-Zeelen1990-18">[18]</a> The <a href="/wiki/Biological_half-life" title="Biological half-life">biological half-life</a> of allylestrenol has been reported to be "several hours" or, presumably in its active form, reportedly about 10 hours.<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a><a href="#cite_note-SahaRoy2000-4">[4]</a> In the blood, unchanged allylestrenol accounted for 15 to 40% of <a href="/wiki/Radioactivity" class="mw-redirect" title="Radioactivity">radioactivity</a>, an unconjugated metabolite accounted for 4 to 10% of radioactivity, and the rest of the radioactivity corresponded to conjugated metabolites.<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a> Allylestrenol is <a href="/wiki/Elimination_(pharmacology)" title="Elimination (pharmacology)">eliminated</a> mainly in <a href="/wiki/Urine" title="Urine">urine</a>, 44% by 24 hours and 67% within 4 days.<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a> It is <a href="/wiki/Excretion" title="Excretion">excreted</a> almost completely as conjugates, with 75% of these being <a href="/wiki/Sulfate" title="Sulfate">sulfate</a> conjugates and 24% being <a href="/wiki/Glucuronide" title="Glucuronide">glucuronide</a> conjugates.<a href="#cite_note-BengtssonTausk1972-1">[1]</a><a href="#cite_note-Thijssen1967-2">[2]</a> <div class="mw-heading mw-heading2"><h2 id="Chemistry">Chemistry</h2>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=10" title="Edit section: Chemistry">edit</a>]</div> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1236090951"><div role="note" class="hatnote navigation-not-searchable">See also: <a href="/wiki/List_of_progestogens" title="List of progestogens">List of progestogens</a></div> Allylestrenol, also known as 3-deketo-17α-allyl-19-nortestosterone or as 17α-allylestr-4-en-17β-ol, is a <a href="/wiki/Synthetic_compound" class="mw-redirect" title="Synthetic compound">synthetic</a> <a href="/wiki/Estrane" title="Estrane">estrane</a> <a href="/wiki/Steroid" title="Steroid">steroid</a> and a <a href="/wiki/Chemical_derivative" class="mw-redirect" title="Chemical derivative">derivative</a> of <a href="/wiki/Testosterone" title="Testosterone">testosterone</a>.<a href="#cite_note-Elks2014-58">[58]</a> It is a member of the estrane subgroup of the <a href="/wiki/19-nortestosterone" class="mw-redirect" title="19-nortestosterone">19-nortestosterone</a> family of progestins,<a href="#cite_note-MVJain2017-59">[59]</a> but unlike most other 19-nortestosterone progestins, is not a derivative of <a href="/wiki/Norethisterone" title="Norethisterone">norethisterone</a> (17α-ethynyl-19-nortestosterone).<a href="#cite_note-Aronson2009-60">[60]</a><a href="#cite_note-BerginkLoonen1985-3">[3]</a><a href="#cite_note-Zeelen1990-18">[18]</a> This is because it possesses an <a href="/wiki/Allyl_group" title="Allyl group">allyl group</a> at the C17α position rather than the usual <a href="/wiki/Ethynyl_group" title="Ethynyl group">ethynyl group</a>.<a href="#cite_note-Aronson2009-60">[60]</a><a href="#cite_note-BerginkLoonen1985-3">[3]</a><a href="#cite_note-Zeelen1990-18">[18]</a> As such, along with <a href="/wiki/Altrenogest" title="Altrenogest">altrenogest</a> (17α-allyl-19-nor-δ9,11-testosterone), allylestrenol is a derivative of <a href="/wiki/17%CE%B1-allyltestosterone" class="mw-redirect" title="17α-allyltestosterone">17α-allyltestosterone</a> rather than of <a href="/wiki/17%CE%B1-ethynyltestosterone" class="mw-redirect" title="17α-ethynyltestosterone">17α-ethynyltestosterone</a>.<a href="#cite_note-Aronson2009-60">[60]</a><a href="#cite_note-BerginkLoonen1985-3">[3]</a><a href="#cite_note-Zeelen1990-18">[18]</a> Allylestrenol is also unique among most 19-nortestosterone progestins in that it lacks the <a href="/wiki/Ketone" title="Ketone">ketone</a> at the C3 position.<a href="#cite_note-Elks2014-58">[58]</a> It shares this property with <a href="/wiki/Lynestrenol" title="Lynestrenol">lynestrenol</a> (17α-ethynylestr-4-en-17β-ol), <a href="/wiki/Desogestrel" title="Desogestrel">desogestrel</a> (11-methylene-17α-ethynyl-18-methylestr-4-en-17β-ol), and the <a href="/wiki/Anabolic%E2%80%93androgenic_steroid" class="mw-redirect" title="Anabolic–androgenic steroid">anabolic–androgenic steroid</a> (AAS) <a href="/wiki/Ethylestrenol" title="Ethylestrenol">ethylestrenol</a> (17α-ethylestr-4-en-17β-ol).<a href="#cite_note-Elks2014-58">[58]</a> Allylestrenol is the C17α allyl and C3 deketo derivative of the AAS <a href="/wiki/Nandrolone" title="Nandrolone">nandrolone</a> (19-nortestosterone), as well as the C17α allyl and C3 deketo <a href="/wiki/Structural_analog" title="Structural analog">analogue</a> of the AAS <a href="/wiki/Normethandrone" title="Normethandrone">normethandrone</a> (17α-methyl-19-nortestosterone) and <a href="/wiki/Norethandrolone" title="Norethandrolone">norethandrolone</a> (17α-methyl-19-nortestosterone).<a href="#cite_note-Elks2014-58">[58]</a> <div class="mw-heading mw-heading3"><h3 id="Synthesis">Synthesis</h3>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=11" title="Edit section: Synthesis">edit</a>]</div> <a href="/wiki/Chemical_synthesis" title="Chemical synthesis">Chemical syntheses</a> of allylestrenol have been published.<a href="#cite_note-Elks2014-58">[58]</a><a href="#cite_note-Publishing2013-19">[19]</a><a href="#cite_note-GunnetDixon2000-61">[61]</a><a href="#cite_note-Springer2013-62">[62]</a><a href="#cite_note-DeWinterSiegman1959-63">[63]</a> <div class="mw-heading mw-heading2"><h2 id="History">History</h2>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=12" title="Edit section: History">edit</a>]</div> Allylestrenol was patented in 1958<a href="#cite_note-Publishing2013-19">[19]</a> and has been marketed for medical use since 1961.<a href="#cite_note-Field-RichardsSnaith1961-20">[20]</a><a href="#cite_note-SimpsonWeiner1997-21">[21]</a><a href="#cite_note-Juta1962-22">[22]</a> It was developed by <a href="/wiki/Organon_International" class="mw-redirect" title="Organon International">Organon Laboratories</a>.<a href="#cite_note-Juta1962-22">[22]</a><a href="#cite_note-SimpsonWeiner1997-21">[21]</a> <div class="mw-heading mw-heading2"><h2 id="Society_and_culture">Society and culture</h2>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=13" title="Edit section: Society and culture">edit</a>]</div> <div class="mw-heading mw-heading3"><h3 id="Generic_names">Generic names</h3>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=14" title="Edit section: Generic names">edit</a>]</div> Allylestrenol is the <a href="/wiki/Generic_term" class="mw-redirect" title="Generic term">generic name</a> of the drug and its <a href="/wiki/International_Nonproprietary_Name" class="mw-redirect" title="International Nonproprietary Name"><abbr title="International Nonproprietary Name">INN</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip International Nonproprietary Name, <a href="/wiki/British_Approved_Name" title="British Approved Name"><abbr title="British Approved Name">BAN</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip British Approved Name, and <a href="/wiki/Japanese_Accepted_Name" title="Japanese Accepted Name"><abbr title="Japanese Accepted Name">JAN</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Japanese Accepted Name, while allylestrénol is its <a href="/wiki/D%C3%A9nomination_Commune_Fran%C3%A7aise" title="Dénomination Commune Française"><abbr title="Dénomination Commune Française">DCF</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Dénomination Commune Française and allilestrenolo is its <a href="/wiki/Denominazione_Comune_Italiana" title="Denominazione Comune Italiana"><abbr title="Denominazione Comune Italiana">DCIT</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Denominazione Comune Italiana.<a href="#cite_note-Elks2014-58">[58]</a><a href="#cite_note-IndexNominum2000-25">[25]</a><a href="#cite_note-MortonHall2012-64">[64]</a><a href="#cite_note-Drugs.com-24">[24]</a> The <a href="/wiki/British_Approved_Name" title="British Approved Name"><abbr title="British Approved Name">BAN</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip British Approved Name was originally allyloestrenol, but it was eventually changed.<a href="#cite_note-Elks2014-58">[58]</a><a href="#cite_note-IndexNominum2000-25">[25]</a><a href="#cite_note-Drugs.com-24">[24]</a> The medication is also known by its developmental code name SC-6393.<a href="#cite_note-Elks2014-58">[58]</a><a href="#cite_note-IndexNominum2000-25">[25]</a><a href="#cite_note-Drugs.com-24">[24]</a> <div class="mw-heading mw-heading3"><h3 id="Brand_names">Brand names</h3>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=15" title="Edit section: Brand names">edit</a>]</div> The major brand names of allylestrenol include Gestanin, Gestanon, Perselin, and Turinal.<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a><a href="#cite_note-Publishing2013-19">[19]</a> It has also been marketed under a variety of other brand names, including Alese, Alilestrenol, Allynol, Allytry, Alynol, Anin, Arandal, Astanol, Cobarenol, Crestanon, Elmolan, Fetugard, Foegard, Fulterm, Gestanin, Gestanin, Gestanol, Gestanyn, Gestin, Geston, Gestormone, Gestrenol, Gravida, Gravidin, Gravinol, Gravion, Gravynon, Gynerol, Gynonys, Iugr, Lestron, Loestrol, Maintane, Meieston, Moresafe, Nidagest, Orageston, Pelias, Preabor, Pregnolin, Pregtenol, Pregular, Prelab, Premaston, Prenolin, Prestrenol, Profar, Progeston, Protanon, and Shegest.<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a><a href="#cite_note-Publishing2013-19">[19]</a> <div class="mw-heading mw-heading3"><h3 id="Availability">Availability</h3>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=16" title="Edit section: Availability">edit</a>]</div> <figure class="mw-halign-right" typeof="mw:File/Thumb"><a href="/wiki/File:Allylestrenol_availability.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Allylestrenol_availability.png/300px-Allylestrenol_availability.png" decoding="async" width="300" height="162" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Allylestrenol_availability.png/450px-Allylestrenol_availability.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Allylestrenol_availability.png/600px-Allylestrenol_availability.png 2x" data-file-width="4000" data-file-height="2155" /></a><figcaption>Availability of allylestrenol in countries throughout the world as of December 2017. Blue is currently marketed, green is formerly marketed.</figcaption></figure> Allylestrenol has been marketed widely throughout the world, including in <a href="/wiki/Europe" title="Europe">Europe</a>, <a href="/wiki/South_Asia" title="South Asia">Southern</a>, <a href="/wiki/Eastern_Asia" class="mw-redirect" title="Eastern Asia">Eastern</a>, and <a href="/wiki/Southeastern_Asia" class="mw-redirect" title="Southeastern Asia">Southeastern Asia</a>, <a href="/wiki/Africa" title="Africa">Africa</a>, <a href="/wiki/Oceania" title="Oceania">Oceania</a>, and <a href="/wiki/Latin_America" title="Latin America">Latin America</a>.<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a> However, although it has been widely marketed in the past, the availability of allylestrenol is relatively limited today.<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a> It appears to still be available in <a href="/wiki/Bangladesh" title="Bangladesh">Bangladesh</a>, the <a href="/wiki/Czech_Republic" title="Czech Republic">Czech Republic</a>, <a href="/wiki/Egypt" title="Egypt">Egypt</a>, <a href="/wiki/Hong_Kong" title="Hong Kong">Hong Kong</a>, <a href="/wiki/India" title="India">India</a>, <a href="/wiki/Indonesia" title="Indonesia">Indonesia</a>, <a href="/wiki/Japan" title="Japan">Japan</a>, <a href="/wiki/Lithuania" title="Lithuania">Lithuania</a>, <a href="/wiki/Malaysia" title="Malaysia">Malaysia</a>, the <a href="/wiki/Philippines" title="Philippines">Philippines</a>, <a href="/wiki/Russia" title="Russia">Russia</a>, <a href="/wiki/Singapore" title="Singapore">Singapore</a>, and <a href="/wiki/Taiwan" title="Taiwan">Taiwan</a>.<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a> Previously, allylestrenol has also been available in <a href="/wiki/Australia" title="Australia">Australia</a>, <a href="/wiki/Austria" title="Austria">Austria</a>, <a href="/wiki/Belgium" title="Belgium">Belgium</a>, <a href="/wiki/Brazil" title="Brazil">Brazil</a>, <a href="/wiki/Germany" title="Germany">Germany</a>, <a href="/wiki/Greece" title="Greece">Greece</a>, <a href="/wiki/Hungary" title="Hungary">Hungary</a>, <a href="/wiki/Italy" title="Italy">Italy</a>, <a href="/wiki/Luxembourg" title="Luxembourg">Luxembourg</a>, <a href="/wiki/Mexico" title="Mexico">Mexico</a>, <a href="/wiki/Poland" title="Poland">Poland</a>, <a href="/wiki/South_Africa" title="South Africa">South Africa</a>, <a href="/wiki/Spain" title="Spain">Spain</a>, <a href="/wiki/Sweden" title="Sweden">Sweden</a>, <a href="/wiki/Switzerland" title="Switzerland">Switzerland</a>, <a href="/wiki/Turkey" title="Turkey">Turkey</a>, <a href="/wiki/Ukraine" title="Ukraine">Ukraine</a>, the <a href="/wiki/United_Kingdom" title="United Kingdom">United Kingdom</a>, and <a href="/wiki/Yugoslavia" title="Yugoslavia">Yugoslavia</a> (now <a href="/wiki/Serbia" title="Serbia">Serbia</a> and <a href="/wiki/Montenegro" title="Montenegro">Montenegro</a>).<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a> However, it seems to have been discontinued in these countries.<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a> It does not seem to have been marketed in the <a href="/wiki/United_States" title="United States">United States</a> or <a href="/wiki/Canada" title="Canada">Canada</a>.<a href="#cite_note-Micromedex-23">[23]</a><a href="#cite_note-Martindale-6">[6]</a><a href="#cite_note-Drugs.com-24">[24]</a><a href="#cite_note-IndexNominum2000-25">[25]</a><div style="clear:both;" class=""></div> <div class="mw-heading mw-heading2"><h2 id="References">References</h2>[<a href="/w/index.php?title=Allylestrenol&action=edit&section=17" title="Edit section: References">edit</a>]</div> <style data-mw-deduplicate="TemplateStyles:r1239543626">.mw-parser-output .reflist{margin-bottom:0.5em;list-style-type:decimal}@media screen{.mw-parser-output .reflist{font-size:90%}}.mw-parser-output .reflist .references{font-size:100%;margin-bottom:0;list-style-type:inherit}.mw-parser-output .reflist-columns-2{column-width:30em}.mw-parser-output .reflist-columns-3{column-width:25em}.mw-parser-output .reflist-columns{margin-top:0.3em}.mw-parser-output .reflist-columns ol{margin-top:0}.mw-parser-output .reflist-columns li{page-break-inside:avoid;break-inside:avoid-column}.mw-parser-output .reflist-upper-alpha{list-style-type:upper-alpha}.mw-parser-output .reflist-upper-roman{list-style-type:upper-roman}.mw-parser-output .reflist-lower-alpha{list-style-type:lower-alpha}.mw-parser-output .reflist-lower-greek{list-style-type:lower-greek}.mw-parser-output .reflist-lower-roman{list-style-type:lower-roman}</style><div class="reflist"> <div class="mw-references-wrap mw-references-columns"><ol class="references"> <li id="cite_note-BengtssonTausk1972-1">^ <a href="#cite_ref-BengtssonTausk1972_1-0">a</a> <a href="#cite_ref-BengtssonTausk1972_1-1">b</a> <a href="#cite_ref-BengtssonTausk1972_1-2">c</a> <a href="#cite_ref-BengtssonTausk1972_1-3">d</a> <a href="#cite_ref-BengtssonTausk1972_1-4">e</a> <a href="#cite_ref-BengtssonTausk1972_1-5">f</a> <a href="#cite_ref-BengtssonTausk1972_1-6">g</a> <a href="#cite_ref-BengtssonTausk1972_1-7">h</a> <a href="#cite_ref-BengtssonTausk1972_1-8">i</a> <a href="#cite_ref-BengtssonTausk1972_1-9">j</a> <a href="#cite_ref-BengtssonTausk1972_1-10">k</a> <a href="#cite_ref-BengtssonTausk1972_1-11">l</a> <style data-mw-deduplicate="TemplateStyles:r1238218222">.mw-parser-output cite.citation{font-style:inherit;word-wrap:break-word}.mw-parser-output .citation q{quotes:"\"""\"""'""'"}.mw-parser-output .citation:target{background-color:rgba(0,127,255,0.133)}.mw-parser-output .id-lock-free.id-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/6/65/Lock-green.svg")right 0.1em center/9px no-repeat}.mw-parser-output .id-lock-limited.id-lock-limited a,.mw-parser-output .id-lock-registration.id-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/d/d6/Lock-gray-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .id-lock-subscription.id-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/a/aa/Lock-red-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/4/4c/Wikisource-logo.svg")right 0.1em center/12px no-repeat}body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-free a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-limited a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-registration a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-subscription a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .cs1-ws-icon a{background-size:contain;padding:0 1em 0 0}.mw-parser-output .cs1-code{color:inherit;background:inherit;border:none;padding:inherit}.mw-parser-output .cs1-hidden-error{display:none;color:var(--color-error,#d33)}.mw-parser-output .cs1-visible-error{color:var(--color-error,#d33)}.mw-parser-output .cs1-maint{display:none;color:#085;margin-left:0.3em}.mw-parser-output .cs1-kern-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right{padding-right:0.2em}.mw-parser-output .citation .mw-selflink{font-weight:inherit}@media screen{.mw-parser-output .cs1-format{font-size:95%}html.skin-theme-clientpref-night .mw-parser-output .cs1-maint{color:#18911f}}@media screen and (prefers-color-scheme:dark){html.skin-theme-clientpref-os .mw-parser-output .cs1-maint{color:#18911f}}</style><cite id="CITEREFBengtssonTausk1972" class="citation book cs1">Bengtsson LP, Tausk M (September 1972). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=Nv5sAAAAMAAJ">Pharmacology of the endocrine system and related drugs: progesterone, progestational drugs and antifertility agents</a>. Pergamon Press. pp. 235–237. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/9780080157450" title="Special:BookSources/9780080157450"><bdi>9780080157450</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Pharmacology+of+the+endocrine+system+and+related+drugs%3A+progesterone%2C+progestational+drugs+and+antifertility+agents&rft.pages=235-237&rft.pub=Pergamon+Press&rft.date=1972-09&rft.isbn=9780080157450&rft.aulast=Bengtsson&rft.aufirst=LP&rft.au=Tausk%2C+M&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DNv5sAAAAMAAJ&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Thijssen1967-2">^ <a href="#cite_ref-Thijssen1967_2-0">a</a> <a href="#cite_ref-Thijssen1967_2-1">b</a> <a href="#cite_ref-Thijssen1967_2-2">c</a> <a href="#cite_ref-Thijssen1967_2-3">d</a> <a href="#cite_ref-Thijssen1967_2-4">e</a> <a href="#cite_ref-Thijssen1967_2-5">f</a> <a href="#cite_ref-Thijssen1967_2-6">g</a> <a href="#cite_ref-Thijssen1967_2-7">h</a> <a href="#cite_ref-Thijssen1967_2-8">i</a> <a href="#cite_ref-Thijssen1967_2-9">j</a> <a href="#cite_ref-Thijssen1967_2-10">k</a> <a href="#cite_ref-Thijssen1967_2-11">l</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFThijssen1967" class="citation thesis cs1">Thijssen JH (1967). Het metabolisme van progestatieve stoffen (Thesis). Rijksuniversiteit te Utrecht.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adissertation&rft.title=Het+metabolisme+van+progestatieve+stoffen&rft.inst=Rijksuniversiteit+te+Utrecht&rft.date=1967&rft.aulast=Thijssen&rft.aufirst=JH&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-BerginkLoonen1985-3">^ <a href="#cite_ref-BerginkLoonen1985_3-0">a</a> <a href="#cite_ref-BerginkLoonen1985_3-1">b</a> <a href="#cite_ref-BerginkLoonen1985_3-2">c</a> <a href="#cite_ref-BerginkLoonen1985_3-3">d</a> <a href="#cite_ref-BerginkLoonen1985_3-4">e</a> <a href="#cite_ref-BerginkLoonen1985_3-5">f</a> <a href="#cite_ref-BerginkLoonen1985_3-6">g</a> <a href="#cite_ref-BerginkLoonen1985_3-7">h</a> <a href="#cite_ref-BerginkLoonen1985_3-8">i</a> <a href="#cite_ref-BerginkLoonen1985_3-9">j</a> <a href="#cite_ref-BerginkLoonen1985_3-10">k</a> <a href="#cite_ref-BerginkLoonen1985_3-11">l</a> <a href="#cite_ref-BerginkLoonen1985_3-12">m</a> <a href="#cite_ref-BerginkLoonen1985_3-13">n</a> <a href="#cite_ref-BerginkLoonen1985_3-14">o</a> <a href="#cite_ref-BerginkLoonen1985_3-15">p</a> <a href="#cite_ref-BerginkLoonen1985_3-16">q</a> <a href="#cite_ref-BerginkLoonen1985_3-17">r</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBerginkLoonenKloosterboer1985" class="citation journal cs1">Bergink EW, Loonen PB, Kloosterboer HJ (August 1985). "Receptor binding of allylestrenol, a progestagen of the 19-nortestosterone series without androgenic properties". Journal of Steroid Biochemistry. 23 (2): 165–168. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2F0022-4731%2885%2990232-8">10.1016/0022-4731(85)90232-8</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/3928974">3928974</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Journal+of+Steroid+Biochemistry&rft.atitle=Receptor+binding+of+allylestrenol%2C+a+progestagen+of+the+19-nortestosterone+series+without+androgenic+properties&rft.volume=23&rft.issue=2&rft.pages=165-168&rft.date=1985-08&rft_id=info%3Adoi%2F10.1016%2F0022-4731%2885%2990232-8&rft_id=info%3Apmid%2F3928974&rft.aulast=Bergink&rft.aufirst=EW&rft.au=Loonen%2C+PB&rft.au=Kloosterboer%2C+HJ&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-SahaRoy2000-4">^ <a href="#cite_ref-SahaRoy2000_4-0">a</a> <a href="#cite_ref-SahaRoy2000_4-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFSahaRoyKakali2000" class="citation journal cs1">Saha A, Roy K, Kakali DE (2000). "Effects of Allylestrenol on Blood Lipids in Relation to its Biological Activity". Indian Journal of Pharmaceutical Sciences. 62 (2): 115.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Indian+Journal+of+Pharmaceutical+Sciences&rft.atitle=Effects+of+Allylestrenol+on+Blood+Lipids+in+Relation+to+its+Biological+Activity&rft.volume=62&rft.issue=2&rft.pages=115&rft.date=2000&rft.aulast=Saha&rft.aufirst=A&rft.au=Roy%2C+K&rft.au=Kakali%2C+DE&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-SuperCYP-5">^ <a href="#cite_ref-SuperCYP_5-0">a</a> <a href="#cite_ref-SuperCYP_5-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="http://bioinformatics.charite.de/supercyp/">"SuperCYP"</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=SuperCYP&rft_id=http%3A%2F%2Fbioinformatics.charite.de%2Fsupercyp%2F&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Martindale-6">^ <a href="#cite_ref-Martindale_6-0">a</a> <a href="#cite_ref-Martindale_6-1">b</a> <a href="#cite_ref-Martindale_6-2">c</a> <a href="#cite_ref-Martindale_6-3">d</a> <a href="#cite_ref-Martindale_6-4">e</a> <a href="#cite_ref-Martindale_6-5">f</a> <a href="#cite_ref-Martindale_6-6">g</a> <a href="#cite_ref-Martindale_6-7">h</a> <a href="#cite_ref-Martindale_6-8">i</a> <a href="#cite_ref-Martindale_6-9">j</a> <a href="#cite_ref-Martindale_6-10">k</a> <a href="#cite_ref-Martindale_6-11">l</a> <a href="#cite_ref-Martindale_6-12">m</a> <a href="#cite_ref-Martindale_6-13">n</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFSweetman2009" class="citation book cs1">Sweetman SC, ed. (2009). <a rel="nofollow" class="external text" href="https://www.medicinescomplete.com/mc/martindale/2009/9023-n.htm">"Sex hormones and their modulators"</a>. Martindale: The Complete Drug Reference (36th ed.). London: Pharmaceutical Press. p. 2082. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-0-85369-840-1" title="Special:BookSources/978-0-85369-840-1"><bdi>978-0-85369-840-1</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=bookitem&rft.atitle=Sex+hormones+and+their+modulators&rft.btitle=Martindale%3A+The+Complete+Drug+Reference&rft.place=London&rft.pages=2082&rft.edition=36th&rft.pub=Pharmaceutical+Press&rft.date=2009&rft.isbn=978-0-85369-840-1&rft_id=https%3A%2F%2Fwww.medicinescomplete.com%2Fmc%2Fmartindale%2F2009%2F9023-n.htm&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid7459930-7">^ <a href="#cite_ref-pmid7459930_7-0">a</a> <a href="#cite_ref-pmid7459930_7-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFCortés-PrietoBoschRocha1980" class="citation journal cs1">Cortés-Prieto J, Bosch AO, Rocha JA (1980). "Allylestrenol: three years of experience with Gestanon in threatened abortion and premature labor". Clinical Therapeutics. 3 (3): 200–208. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/7459930">7459930</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Clinical+Therapeutics&rft.atitle=Allylestrenol%3A+three+years+of+experience+with+Gestanon+in+threatened+abortion+and+premature+labor&rft.volume=3&rft.issue=3&rft.pages=200-208&rft.date=1980&rft_id=info%3Apmid%2F7459930&rft.aulast=Cort%C3%A9s-Prieto&rft.aufirst=J&rft.au=Bosch%2C+AO&rft.au=Rocha%2C+JA&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-:0-8">^ <a href="#cite_ref-:0_8-0">a</a> <a href="#cite_ref-:0_8-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFHaasHathawayRamsey2019" class="citation journal cs1">Haas DM, Hathaway TJ, Ramsey PS (November 2019). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953238">"Progestogen for preventing miscarriage in women with recurrent miscarriage of unclear etiology"</a>. The Cochrane Database of Systematic Reviews. 2019 (11). <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2F14651858.CD003511.pub5">10.1002/14651858.CD003511.pub5</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a> <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953238">6953238</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/31745982">31745982</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=The+Cochrane+Database+of+Systematic+Reviews&rft.atitle=Progestogen+for+preventing+miscarriage+in+women+with+recurrent+miscarriage+of+unclear+etiology&rft.volume=2019&rft.issue=11&rft.date=2019-11&rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC6953238%23id-name%3DPMC&rft_id=info%3Apmid%2F31745982&rft_id=info%3Adoi%2F10.1002%2F14651858.CD003511.pub5&rft.aulast=Haas&rft.aufirst=DM&rft.au=Hathaway%2C+TJ&rft.au=Ramsey%2C+PS&rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC6953238&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid1722627-9">^ <a href="#cite_ref-pmid1722627_9-0">a</a> <a href="#cite_ref-pmid1722627_9-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFKanimotoOkada1991" class="citation journal cs1 cs1-prop-foreign-lang-source">Kanimoto Y, Okada K (November 1991). "[Antiandrogen therapy of benign prostatic hyperplasia--review of the agents evaluation of the clinical results]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 37 (11): 1423–1428. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/1722627">1722627</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BAntiandrogen+therapy+of+benign+prostatic+hyperplasia--review+of+the+agents+evaluation+of+the+clinical+results%5D&rft.volume=37&rft.issue=11&rft.pages=1423-1428&rft.date=1991-11&rft_id=info%3Apmid%2F1722627&rft.aulast=Kanimoto&rft.aufirst=Y&rft.au=Okada%2C+K&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid1722628-10">^ <a href="#cite_ref-pmid1722628_10-0">a</a> <a href="#cite_ref-pmid1722628_10-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFUmeda1991" class="citation journal cs1 cs1-prop-foreign-lang-source">Umeda K (November 1991). "[Clinical results and problems of anti-androgen therapy of benign prostatic hypertrophy]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 37 (11): 1429–1433. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/1722628">1722628</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BClinical+results+and+problems+of+anti-androgen+therapy+of+benign+prostatic+hypertrophy%5D&rft.volume=37&rft.issue=11&rft.pages=1429-1433&rft.date=1991-11&rft_id=info%3Apmid%2F1722628&rft.aulast=Umeda&rft.aufirst=K&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid12534901-11">^ <a href="#cite_ref-pmid12534901_11-0">a</a> <a href="#cite_ref-pmid12534901_11-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFIshizukaNishizawaHiraoOhshima2002" class="citation journal cs1">Ishizuka O, Nishizawa O, Hirao Y, Ohshima S (November 2002). <a rel="nofollow" class="external text" href="https://doi.org/10.1046%2Fj.1442-2042.2002.00539.x">"Evidence-based meta-analysis of pharmacotherapy for benign prostatic hypertrophy"</a>. International Journal of Urology. 9 (11): 607–612. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1046%2Fj.1442-2042.2002.00539.x">10.1046/j.1442-2042.2002.00539.x</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/12534901">12534901</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=International+Journal+of+Urology&rft.atitle=Evidence-based+meta-analysis+of+pharmacotherapy+for+benign+prostatic+hypertrophy&rft.volume=9&rft.issue=11&rft.pages=607-612&rft.date=2002-11&rft_id=info%3Adoi%2F10.1046%2Fj.1442-2042.2002.00539.x&rft_id=info%3Apmid%2F12534901&rft.aulast=Ishizuka&rft.aufirst=O&rft.au=Nishizawa%2C+O&rft.au=Hirao%2C+Y&rft.au=Ohshima%2C+S&rft_id=https%3A%2F%2Fdoi.org%2F10.1046%252Fj.1442-2042.2002.00539.x&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Muller1998-12">^ <a href="#cite_ref-Muller1998_12-0">a</a> <a href="#cite_ref-Muller1998_12-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMuller1998" class="citation book cs1">Muller (19 June 1998). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=2HBPHmclMWIC&pg=PA545">European Drug Index: European Drug Registrations</a> (Fourth ed.). CRC Press. pp. 545–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-3-7692-2114-5" title="Special:BookSources/978-3-7692-2114-5"><bdi>978-3-7692-2114-5</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=European+Drug+Index%3A+European+Drug+Registrations&rft.pages=545-&rft.edition=Fourth&rft.pub=CRC+Press&rft.date=1998-06-19&rft.isbn=978-3-7692-2114-5&rft.au=Muller&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3D2HBPHmclMWIC%26pg%3DPA545&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Seth2009-13"><a href="#cite_ref-Seth2009_13-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFGangulyBanoSeth2009" class="citation book cs1">Ganguly NK, Bano R, Seth SD (18 November 2009). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=51ozlZRBvQwC&pg=RA1-PA71">"Drug Discovery and Development"</a>. In Seth SD, Seth V (eds.). Textbook Of Pharmacology. Elsevier India. pp. 1–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-81-312-1158-8" title="Special:BookSources/978-81-312-1158-8"><bdi>978-81-312-1158-8</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=bookitem&rft.atitle=Drug+Discovery+and+Development&rft.btitle=Textbook+Of+Pharmacology&rft.pages=1-&rft.pub=Elsevier+India&rft.date=2009-11-18&rft.isbn=978-81-312-1158-8&rft.aulast=Ganguly&rft.aufirst=NK&rft.au=Bano%2C+R&rft.au=Seth%2C+SD&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3D51ozlZRBvQwC%26pg%3DRA1-PA71&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Borglin1960-14">^ <a href="#cite_ref-Borglin1960_14-0">a</a> <a href="#cite_ref-Borglin1960_14-1">b</a> <a href="#cite_ref-Borglin1960_14-2">c</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBorglin1960" class="citation journal cs1">Borglin NE (1960). "Clinical Evaluation of the Progestational Effect of Allylestrenol". European Journal of Endocrinology. 35 (4 Suppl): NP–S15. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1530%2Facta.0.XXXVS0NP">10.1530/acta.0.XXXVS0NP</a>. <a href="/wiki/ISSN_(identifier)" class="mw-redirect" title="ISSN (identifier)">ISSN</a> <a rel="nofollow" class="external text" href="https://search.worldcat.org/issn/0804-4643">0804-4643</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=European+Journal+of+Endocrinology&rft.atitle=Clinical+Evaluation+of+the+Progestational+Effect+of+Allylestrenol&rft.volume=35&rft.issue=4+Suppl&rft.pages=NP-S15&rft.date=1960&rft_id=info%3Adoi%2F10.1530%2Facta.0.XXXVS0NP&rft.issn=0804-4643&rft.aulast=Borglin&rft.aufirst=NE&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid13699366-15">^ <a href="#cite_ref-pmid13699366_15-0">a</a> <a href="#cite_ref-pmid13699366_15-1">b</a> <a href="#cite_ref-pmid13699366_15-2">c</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFField-RichardsSnaith1961" class="citation journal cs1">Field-Richards S, Snaith L (January 1961). "Allylestrenol: a new oral progestogen". Lancet. 1 (7169): 134–136. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fs0140-6736%2861%2991310-1">10.1016/s0140-6736(61)91310-1</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/13699366">13699366</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Lancet&rft.atitle=Allylestrenol%3A+a+new+oral+progestogen&rft.volume=1&rft.issue=7169&rft.pages=134-136&rft.date=1961-01&rft_id=info%3Adoi%2F10.1016%2Fs0140-6736%2861%2991310-1&rft_id=info%3Apmid%2F13699366&rft.aulast=Field-Richards&rft.aufirst=S&rft.au=Snaith%2C+L&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Madjerekde_Visser1960-16">^ <a href="#cite_ref-Madjerekde_Visser1960_16-0">a</a> <a href="#cite_ref-Madjerekde_Visser1960_16-1">b</a> <a href="#cite_ref-Madjerekde_Visser1960_16-2">c</a> <a href="#cite_ref-Madjerekde_Visser1960_16-3">d</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMadjerekDe_VisserVan_Der_ViesOverbeek1960" class="citation journal cs1">Madjerek Z, De Visser J, Van Der Vies J, Overbeek GA (September 1960). "Allylestrenol, a pregnancy maintaining oral gestagen". Acta Endocrinologica. 35 (I): 8–19. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1530%2Facta.0.XXXV0008">10.1530/acta.0.XXXV0008</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/13765069">13765069</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Acta+Endocrinologica&rft.atitle=Allylestrenol%2C+a+pregnancy+maintaining+oral+gestagen&rft.volume=35&rft.issue=I&rft.pages=8-19&rft.date=1960-09&rft_id=info%3Adoi%2F10.1530%2Facta.0.XXXV0008&rft_id=info%3Apmid%2F13765069&rft.aulast=Madjerek&rft.aufirst=Z&rft.au=De+Visser%2C+J&rft.au=Van+Der+Vies%2C+J&rft.au=Overbeek%2C+GA&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid18395441-17">^ <a href="#cite_ref-pmid18395441_17-0">a</a> <a href="#cite_ref-pmid18395441_17-1">b</a> <a href="#cite_ref-pmid18395441_17-2">c</a> <a href="#cite_ref-pmid18395441_17-3">d</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMcRobbHandelsmanKazlauskasWilkinson2008" class="citation journal cs1">McRobb L, Handelsman DJ, Kazlauskas R, Wilkinson S, McLeod MD, Heather AK (May 2008). "Structure-activity relationships of synthetic progestins in a yeast-based in vitro androgen bioassay". The Journal of Steroid Biochemistry and Molecular Biology. 110 (1–2): 39–47. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.jsbmb.2007.10.008">10.1016/j.jsbmb.2007.10.008</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/18395441">18395441</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a> <a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:5612000">5612000</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=The+Journal+of+Steroid+Biochemistry+and+Molecular+Biology&rft.atitle=Structure-activity+relationships+of+synthetic+progestins+in+a+yeast-based+in+vitro+androgen+bioassay&rft.volume=110&rft.issue=1%E2%80%932&rft.pages=39-47&rft.date=2008-05&rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A5612000%23id-name%3DS2CID&rft_id=info%3Apmid%2F18395441&rft_id=info%3Adoi%2F10.1016%2Fj.jsbmb.2007.10.008&rft.aulast=McRobb&rft.aufirst=L&rft.au=Handelsman%2C+DJ&rft.au=Kazlauskas%2C+R&rft.au=Wilkinson%2C+S&rft.au=McLeod%2C+MD&rft.au=Heather%2C+AK&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Zeelen1990-18">^ <a href="#cite_ref-Zeelen1990_18-0">a</a> <a href="#cite_ref-Zeelen1990_18-1">b</a> <a href="#cite_ref-Zeelen1990_18-2">c</a> <a href="#cite_ref-Zeelen1990_18-3">d</a> <a href="#cite_ref-Zeelen1990_18-4">e</a> <a href="#cite_ref-Zeelen1990_18-5">f</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFZeelen1990" class="citation book cs1">Zeelen FJ (1990). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=px9tAAAAMAAJ">Medicinal chemistry of steroids</a>. Elsevier Science Limited. pp. 108–109. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-0-444-88727-6" title="Special:BookSources/978-0-444-88727-6"><bdi>978-0-444-88727-6</bdi></a>. <q>Other examples are allylestrenol (42), a pro-drug converted to the 3-keto analogue (43), which is used in the treatment of threatened abortion [78,79] and altrenogest (44), used in sows and mares to suppress ovulation and estrus behaviour [80]. [...] Progestins with a 17a-allyl side chain: (42) allylestrenol, (43), (44) altrenogest.</q></cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Medicinal+chemistry+of+steroids&rft.pages=108-109&rft.pub=Elsevier+Science+Limited&rft.date=1990&rft.isbn=978-0-444-88727-6&rft.aulast=Zeelen&rft.aufirst=FJ&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3Dpx9tAAAAMAAJ&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Publishing2013-19">^ <a href="#cite_ref-Publishing2013_19-0">a</a> <a href="#cite_ref-Publishing2013_19-1">b</a> <a href="#cite_ref-Publishing2013_19-2">c</a> <a href="#cite_ref-Publishing2013_19-3">d</a> <a href="#cite_ref-Publishing2013_19-4">e</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFWilliam_Andrew_Publishing2013" class="citation book cs1">William Andrew Publishing (22 October 2013). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=_J2ti4EkYpkC&pg=PA170">Pharmaceutical Manufacturing Encyclopedia, 3rd Edition</a>. Elsevier. pp. 170–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-0-8155-1856-3" title="Special:BookSources/978-0-8155-1856-3"><bdi>978-0-8155-1856-3</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Pharmaceutical+Manufacturing+Encyclopedia%2C+3rd+Edition&rft.pages=170-&rft.pub=Elsevier&rft.date=2013-10-22&rft.isbn=978-0-8155-1856-3&rft.au=William+Andrew+Publishing&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3D_J2ti4EkYpkC%26pg%3DPA170&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Field-RichardsSnaith1961-20">^ <a href="#cite_ref-Field-RichardsSnaith1961_20-0">a</a> <a href="#cite_ref-Field-RichardsSnaith1961_20-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFField-RichardsSnaith1961" class="citation journal cs1">Field-Richards S, Snaith L (January 1961). "Allylestrenol: a new oral progestogen". Lancet. 1 (7169): 134–136. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2FS0140-6736%2861%2991310-1">10.1016/S0140-6736(61)91310-1</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/13699366">13699366</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Lancet&rft.atitle=Allylestrenol%3A+a+new+oral+progestogen&rft.volume=1&rft.issue=7169&rft.pages=134-136&rft.date=1961-01&rft_id=info%3Adoi%2F10.1016%2FS0140-6736%2861%2991310-1&rft_id=info%3Apmid%2F13699366&rft.aulast=Field-Richards&rft.aufirst=S&rft.au=Snaith%2C+L&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-SimpsonWeiner1997-21">^ <a href="#cite_ref-SimpsonWeiner1997_21-0">a</a> <a href="#cite_ref-SimpsonWeiner1997_21-1">b</a> <a href="#cite_ref-SimpsonWeiner1997_21-2">c</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFSimpsonWeiner1997" class="citation book cs1">Simpson JA, Weiner ES (1997). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=gUGcAQAAQBAJ&pg=PA36">Oxford English Dictionary Additions Series</a>. Clarendon Press. pp. 36–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-0-19-860027-5" title="Special:BookSources/978-0-19-860027-5"><bdi>978-0-19-860027-5</bdi></a>. <q>1961 Lancet 21 Jan. 135/1 Allylestrenol ('Gestanin', Organon)..seems to be completely free from androgenic activity. 1962 Med. Jrnl. Austral. 8 Sept. 375/2 Each tablet of the combined hormone preparation, 'Premenquil', contains 5 mg. of allyloestrenol. [...]</q></cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Oxford+English+Dictionary+Additions+Series&rft.pages=36-&rft.pub=Clarendon+Press&rft.date=1997&rft.isbn=978-0-19-860027-5&rft.aulast=Simpson&rft.aufirst=JA&rft.au=Weiner%2C+ES&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DgUGcAQAAQBAJ%26pg%3DPA36&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Juta1962-22">^ <a href="#cite_ref-Juta1962_22-0">a</a> <a href="#cite_ref-Juta1962_22-1">b</a> <a href="#cite_ref-Juta1962_22-2">c</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation book cs1"><a rel="nofollow" class="external text" href="https://books.google.com/books?id=QORDAQAAIAAJ">Medical Proceedings: A South African Journal for the Advancement of Medical Science</a>. Juta and Company. 1962. <q>Just released in South Africa is Gestanin, Organon Laboratories' new safe oral progestogen. Gestanin is allylestrenol, one of a new group of steroids synthesized by Organon.</q></cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Medical+Proceedings%3A+A+South+African+Journal+for+the+Advancement+of+Medical+Science&rft.pub=Juta+and+Company&rft.date=1962&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DQORDAQAAIAAJ&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Micromedex-23">^ <a href="#cite_ref-Micromedex_23-0">a</a> <a href="#cite_ref-Micromedex_23-1">b</a> <a href="#cite_ref-Micromedex_23-2">c</a> <a href="#cite_ref-Micromedex_23-3">d</a> <a href="#cite_ref-Micromedex_23-4">e</a> <a href="#cite_ref-Micromedex_23-5">f</a> <a href="#cite_ref-Micromedex_23-6">g</a> <a href="#cite_ref-Micromedex_23-7">h</a> <a href="#cite_ref-Micromedex_23-8">i</a> <a href="#cite_ref-Micromedex_23-9">j</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="http://www.micromedexsolutions.com/micromedex2/librarian/">"Micromedex Products: Please Login"</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=Micromedex+Products%3A+Please+Login&rft_id=http%3A%2F%2Fwww.micromedexsolutions.com%2Fmicromedex2%2Flibrarian%2F&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Drugs.com-24">^ <a href="#cite_ref-Drugs.com_24-0">a</a> <a href="#cite_ref-Drugs.com_24-1">b</a> <a href="#cite_ref-Drugs.com_24-2">c</a> <a href="#cite_ref-Drugs.com_24-3">d</a> <a href="#cite_ref-Drugs.com_24-4">e</a> <a href="#cite_ref-Drugs.com_24-5">f</a> <a href="#cite_ref-Drugs.com_24-6">g</a> <a href="#cite_ref-Drugs.com_24-7">h</a> <a href="#cite_ref-Drugs.com_24-8">i</a> <a href="#cite_ref-Drugs.com_24-9">j</a> <a href="#cite_ref-Drugs.com_24-10">k</a> <a href="#cite_ref-Drugs.com_24-11">l</a> <a href="#cite_ref-Drugs.com_24-12">m</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="https://www.drugs.com/international/allylestrenol.html">"Allylestrenol"</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=Allylestrenol&rft_id=https%3A%2F%2Fwww.drugs.com%2Finternational%2Fallylestrenol.html&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-IndexNominum2000-25">^ <a href="#cite_ref-IndexNominum2000_25-0">a</a> <a href="#cite_ref-IndexNominum2000_25-1">b</a> <a href="#cite_ref-IndexNominum2000_25-2">c</a> <a href="#cite_ref-IndexNominum2000_25-3">d</a> <a href="#cite_ref-IndexNominum2000_25-4">e</a> <a href="#cite_ref-IndexNominum2000_25-5">f</a> <a href="#cite_ref-IndexNominum2000_25-6">g</a> <a href="#cite_ref-IndexNominum2000_25-7">h</a> <a href="#cite_ref-IndexNominum2000_25-8">i</a> <a href="#cite_ref-IndexNominum2000_25-9">j</a> <a href="#cite_ref-IndexNominum2000_25-10">k</a> <a href="#cite_ref-IndexNominum2000_25-11">l</a> <a href="#cite_ref-IndexNominum2000_25-12">m</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation book cs1"><a rel="nofollow" class="external text" href="https://books.google.com/books?id=5GpcTQD_L2oC&pg=PA29">Index Nominum 2000: International Drug Directory</a>. Taylor & Francis. January 2000. pp. 29–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-3-88763-075-1" title="Special:BookSources/978-3-88763-075-1"><bdi>978-3-88763-075-1</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Index+Nominum+2000%3A+International+Drug+Directory&rft.pages=29-&rft.pub=Taylor+%26+Francis&rft.date=2000-01&rft.isbn=978-3-88763-075-1&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3D5GpcTQD_L2oC%26pg%3DPA29&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid3609436-26"><a href="#cite_ref-pmid3609436_26-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBirkenfeldNavotEzraRon1987" class="citation journal cs1">Birkenfeld A, Navot D, Ezra Y, Ron A, Schenker JG (July 1987). "The effect of estradiol valerate and allylestrenol on endometrial transformation in hypergonadotropic hypogonadic women". European Journal of Obstetrics, Gynecology, and Reproductive Biology. 25 (3): 221–229. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2F0028-2243%2887%2990102-X">10.1016/0028-2243(87)90102-X</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/3609436">3609436</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=European+Journal+of+Obstetrics%2C+Gynecology%2C+and+Reproductive+Biology&rft.atitle=The+effect+of+estradiol+valerate+and+allylestrenol+on+endometrial+transformation+in+hypergonadotropic+hypogonadic+women&rft.volume=25&rft.issue=3&rft.pages=221-229&rft.date=1987-07&rft_id=info%3Adoi%2F10.1016%2F0028-2243%2887%2990102-X&rft_id=info%3Apmid%2F3609436&rft.aulast=Birkenfeld&rft.aufirst=A&rft.au=Navot%2C+D&rft.au=Ezra%2C+Y&rft.au=Ron%2C+A&rft.au=Schenker%2C+JG&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid1473164-27"><a href="#cite_ref-pmid1473164_27-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBartákRozprávkaBlovský1992" class="citation journal cs1 cs1-prop-foreign-lang-source">Barták A, Rozprávka M, Blovský J (October 1992). "[Lynestrenol and allylestrenol in the therapy of postmenopausal hot flushes]". Ceskoslovenska Gynekologie (in Czech). 57 (8): 408–413. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/1473164">1473164</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Ceskoslovenska+Gynekologie&rft.atitle=%5BLynestrenol+and+allylestrenol+in+the+therapy+of+postmenopausal+hot+flushes%5D&rft.volume=57&rft.issue=8&rft.pages=408-413&rft.date=1992-10&rft_id=info%3Apmid%2F1473164&rft.aulast=Bart%C3%A1k&rft.aufirst=A&rft.au=Rozpr%C3%A1vka%2C+M&rft.au=Blovsk%C3%BD%2C+J&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid6203385-28">^ <a href="#cite_ref-pmid6203385_28-0">a</a> <a href="#cite_ref-pmid6203385_28-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFYamanakaKosakuMakinoShida1983" class="citation journal cs1 cs1-prop-foreign-lang-source">Yamanaka H, Kosaku N, Makino T, Shida K (September 1983). "[Fundamental and clinical study of the anti-prostatic effect of allylestrenol]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 29 (9): 1133–1145. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/6203385">6203385</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BFundamental+and+clinical+study+of+the+anti-prostatic+effect+of+allylestrenol%5D&rft.volume=29&rft.issue=9&rft.pages=1133-1145&rft.date=1983-09&rft_id=info%3Apmid%2F6203385&rft.aulast=Yamanaka&rft.aufirst=H&rft.au=Kosaku%2C+N&rft.au=Makino%2C+T&rft.au=Shida%2C+K&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid2425610-29"><a href="#cite_ref-pmid2425610_29-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFTajimaAsoUshiyamaHata1986" class="citation journal cs1 cs1-prop-foreign-lang-source">Tajima A, Aso Y, Ushiyama T, Hata M, Kambayashi T, Ohmi Y, et al. (March 1986). "[Clinical effect of allylestrenol on benign prostatic hypertrophy]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 32 (3): 477–485. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/2425610">2425610</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BClinical+effect+of+allylestrenol+on+benign+prostatic+hypertrophy%5D&rft.volume=32&rft.issue=3&rft.pages=477-485&rft.date=1986-03&rft_id=info%3Apmid%2F2425610&rft.aulast=Tajima&rft.aufirst=A&rft.au=Aso%2C+Y&rft.au=Ushiyama%2C+T&rft.au=Hata%2C+M&rft.au=Kambayashi%2C+T&rft.au=Ohmi%2C+Y&rft.au=Masuda%2C+H&rft.au=Nakahara%2C+M&rft.au=Kitagawa%2C+M&rft.au=Suzuki%2C+A&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid2425611-30"><a href="#cite_ref-pmid2425611_30-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFKohriKuritaIguchiKataoka1986" class="citation journal cs1 cs1-prop-foreign-lang-source">Kohri K, Kurita T, Iguchi M, Kataoka K (March 1986). "[Clinical effects of allylestrenol on prostatic hypertrophy]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 32 (3): 486–492. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/2425611">2425611</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BClinical+effects+of+allylestrenol+on+prostatic+hypertrophy%5D&rft.volume=32&rft.issue=3&rft.pages=486-492&rft.date=1986-03&rft_id=info%3Apmid%2F2425611&rft.aulast=Kohri&rft.aufirst=K&rft.au=Kurita%2C+T&rft.au=Iguchi%2C+M&rft.au=Kataoka%2C+K&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid2426932-31">^ <a href="#cite_ref-pmid2426932_31-0">a</a> <a href="#cite_ref-pmid2426932_31-1">b</a> <a href="#cite_ref-pmid2426932_31-2">c</a> <a href="#cite_ref-pmid2426932_31-3">d</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFShidaKoyanagiKawakuraNishida1986" class="citation journal cs1 cs1-prop-foreign-lang-source">Shida K, Koyanagi T, Kawakura K, Nishida T, Kumamoto Y, Orikasa S, et al. (April 1986). "[Clinical effects of allylestrenol on benign prostatic hypertrophy by double-blind method]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 32 (4): 625–648. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/2426932">2426932</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BClinical+effects+of+allylestrenol+on+benign+prostatic+hypertrophy+by+double-blind+method%5D&rft.volume=32&rft.issue=4&rft.pages=625-648&rft.date=1986-04&rft_id=info%3Apmid%2F2426932&rft.aulast=Shida&rft.aufirst=K&rft.au=Koyanagi%2C+T&rft.au=Kawakura%2C+K&rft.au=Nishida%2C+T&rft.au=Kumamoto%2C+Y&rft.au=Orikasa%2C+S&rft.au=Sato%2C+S&rft.au=Takeda%2C+M&rft.au=Yamanaka%2C+H&rft.au=Shimazaki%2C+J&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid2426933-32">^ <a href="#cite_ref-pmid2426933_32-0">a</a> <a href="#cite_ref-pmid2426933_32-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFOhyamaTanifujiHaraguchiFujii1986" class="citation journal cs1 cs1-prop-foreign-lang-source">Ohyama M, Tanifuji T, Haraguchi C, Fujii N, Higaki Y, Yoshida H, Imamura K (April 1986). "[Clinical study of allylestrenol (Org AL-25) on patients with prostatic hypertrophy--transrectal ultrasonography and urodynamic examination]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 32 (4): 649–659. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/2426933">2426933</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BClinical+study+of+allylestrenol+%28Org+AL-25%29+on+patients+with+prostatic+hypertrophy--transrectal+ultrasonography+and+urodynamic+examination%5D&rft.volume=32&rft.issue=4&rft.pages=649-659&rft.date=1986-04&rft_id=info%3Apmid%2F2426933&rft.aulast=Ohyama&rft.aufirst=M&rft.au=Tanifuji%2C+T&rft.au=Haraguchi%2C+C&rft.au=Fujii%2C+N&rft.au=Higaki%2C+Y&rft.au=Yoshida%2C+H&rft.au=Imamura%2C+K&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid2435122-33">^ <a href="#cite_ref-pmid2435122_33-0">a</a> <a href="#cite_ref-pmid2435122_33-1">b</a> <a href="#cite_ref-pmid2435122_33-2">c</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFKatayamaUmedaKazama1986" class="citation journal cs1 cs1-prop-foreign-lang-source">Katayama T, Umeda K, Kazama T (November 1986). "[Hormonal environment and antiandrogenic treatment in benign prostatic hypertrophy]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 32 (11): 1584–1589. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/2435122">2435122</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BHormonal+environment+and+antiandrogenic+treatment+in+benign+prostatic+hypertrophy%5D&rft.volume=32&rft.issue=11&rft.pages=1584-1589&rft.date=1986-11&rft_id=info%3Apmid%2F2435122&rft.aulast=Katayama&rft.aufirst=T&rft.au=Umeda%2C+K&rft.au=Kazama%2C+T&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid1693037-34">^ <a href="#cite_ref-pmid1693037_34-0">a</a> <a href="#cite_ref-pmid1693037_34-1">b</a> <a href="#cite_ref-pmid1693037_34-2">c</a> <a href="#cite_ref-pmid1693037_34-3">d</a> <a href="#cite_ref-pmid1693037_34-4">e</a> <a href="#cite_ref-pmid1693037_34-5">f</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFKumamotoYamaguchiSatoSuzuki1990" class="citation journal cs1 cs1-prop-foreign-lang-source">Kumamoto Y, Yamaguchi Y, Sato Y, Suzuki R, Tanda H, Kato S, et al. (February 1990). "[Effects of anti-androgens on sexual function. Double-blind comparative studies on allylestrenol and chlormadinone acetate Part I: Nocturnal penile tumescence monitoring]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 36 (2): 213–226. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/1693037">1693037</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BEffects+of+anti-androgens+on+sexual+function.+Double-blind+comparative+studies+on+allylestrenol+and+chlormadinone+acetate+Part+I%3A+Nocturnal+penile+tumescence+monitoring%5D&rft.volume=36&rft.issue=2&rft.pages=213-226&rft.date=1990-02&rft_id=info%3Apmid%2F1693037&rft.aulast=Kumamoto&rft.aufirst=Y&rft.au=Yamaguchi%2C+Y&rft.au=Sato%2C+Y&rft.au=Suzuki%2C+R&rft.au=Tanda%2C+H&rft.au=Kato%2C+S&rft.au=Mori%2C+K&rft.au=Matsumoto%2C+H&rft.au=Maki%2C+A&rft.au=Kadono%2C+M&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid1693038-35">^ <a href="#cite_ref-pmid1693038_35-0">a</a> <a href="#cite_ref-pmid1693038_35-1">b</a> <a href="#cite_ref-pmid1693038_35-2">c</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFKumamotoYamaguchiSatoSuzuki1990" class="citation journal cs1 cs1-prop-foreign-lang-source">Kumamoto Y, Yamaguchi Y, Sato Y, Suzuki R, Tanda H, Kato S, et al. (February 1990). <a rel="nofollow" class="external text" href="https://repository.kulib.kyoto-u.ac.jp/dspace/bitstream/2433/116823/1/36_213.pdf">"[Effects of anti-androgens on sexual function. Double-blind comparative studies on allylestrenol and chlormadinone acetate. Part II: Self-assessment questionnaire method]"</a> (PDF). Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 36 (2): 227–244. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/1693038">1693038</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BEffects+of+anti-androgens+on+sexual+function.+Double-blind+comparative+studies+on+allylestrenol+and+chlormadinone+acetate.+Part+II%3A+Self-assessment+questionnaire+method%5D&rft.volume=36&rft.issue=2&rft.pages=227-244&rft.date=1990-02&rft_id=info%3Apmid%2F1693038&rft.aulast=Kumamoto&rft.aufirst=Y&rft.au=Yamaguchi%2C+Y&rft.au=Sato%2C+Y&rft.au=Suzuki%2C+R&rft.au=Tanda%2C+H&rft.au=Kato%2C+S&rft.au=Mori%2C+K&rft.au=Matsumoto%2C+H&rft.au=Maki%2C+A&rft.au=Kadono%2C+M&rft_id=https%3A%2F%2Frepository.kulib.kyoto-u.ac.jp%2Fdspace%2Fbitstream%2F2433%2F116823%2F1%2F36_213.pdf&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid1384295-36"><a href="#cite_ref-pmid1384295_36-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFTsujiAriyoshiNakamuraMichinaga1992" class="citation journal cs1 cs1-prop-foreign-lang-source">Tsuji Y, Ariyoshi A, Nakamura H, Michinaga S, Tomita Y, Ohmori A, et al. (August 1992). "[Antiandrogen therapy of benign prostatic hypertrophy: clinical effects of allylestrenol evaluated by transrectal ultrasonographic measurement]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 38 (8): 961–966. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/1384295">1384295</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BAntiandrogen+therapy+of+benign+prostatic+hypertrophy%3A+clinical+effects+of+allylestrenol+evaluated+by+transrectal+ultrasonographic+measurement%5D&rft.volume=38&rft.issue=8&rft.pages=961-966&rft.date=1992-08&rft_id=info%3Apmid%2F1384295&rft.aulast=Tsuji&rft.aufirst=Y&rft.au=Ariyoshi%2C+A&rft.au=Nakamura%2C+H&rft.au=Michinaga%2C+S&rft.au=Tomita%2C+Y&rft.au=Ohmori%2C+A&rft.au=Tahara%2C+H&rft.au=Yamashita%2C+Y&rft.au=Fujisawa%2C+Y&rft.au=Kajiwara%2C+I&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid7689782-37">^ <a href="#cite_ref-pmid7689782_37-0">a</a> <a href="#cite_ref-pmid7689782_37-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFFukuokaIshibashiShibaTuchiya1993" class="citation journal cs1 cs1-prop-foreign-lang-source">Fukuoka H, Ishibashi Y, Shiba T, Tuchiya F, Sakanishi S (July 1993). "[Clinical study of allylestrenol (Perselin) on patients with prostatic hypertrophy]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 39 (7): 679–683. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/7689782">7689782</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BClinical+study+of+allylestrenol+%28Perselin%29+on+patients+with+prostatic+hypertrophy%5D&rft.volume=39&rft.issue=7&rft.pages=679-683&rft.date=1993-07&rft_id=info%3Apmid%2F7689782&rft.aulast=Fukuoka&rft.aufirst=H&rft.au=Ishibashi%2C+Y&rft.au=Shiba%2C+T&rft.au=Tuchiya%2C+F&rft.au=Sakanishi%2C+S&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid7513937-38">^ <a href="#cite_ref-pmid7513937_38-0">a</a> <a href="#cite_ref-pmid7513937_38-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFIguchiIkeuchiKaiYoshida1994" class="citation journal cs1 cs1-prop-foreign-lang-source">Iguchi H, Ikeuchi T, Kai Y, Yoshida H (March 1994). "[Influence of anti-androgen therapy for prostatic hypertrophy on lipid metabolism]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 40 (3): 215–219. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/7513937">7513937</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BInfluence+of+anti-androgen+therapy+for+prostatic+hypertrophy+on+lipid+metabolism%5D&rft.volume=40&rft.issue=3&rft.pages=215-219&rft.date=1994-03&rft_id=info%3Apmid%2F7513937&rft.aulast=Iguchi&rft.aufirst=H&rft.au=Ikeuchi%2C+T&rft.au=Kai%2C+Y&rft.au=Yoshida%2C+H&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid7541089-39">^ <a href="#cite_ref-pmid7541089_39-0">a</a> <a href="#cite_ref-pmid7541089_39-1">b</a> <a href="#cite_ref-pmid7541089_39-2">c</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFHoritaKumamotoSatohSuzuki1995" class="citation journal cs1 cs1-prop-foreign-lang-source">Horita H, Kumamoto Y, Satoh Y, Suzuki N, Wada H, Shibuya A, et al. (May 1995). <a rel="nofollow" class="external text" href="https://doi.org/10.5980%2Fjpnjurol1989.86.1044">"[The preventive effect of indeloxazine hydrochloride to the sexual dysfunction caused by anti-androgenergic agent (allylestrenol)]"</a>. Nihon Hinyokika Gakkai Zasshi. The Japanese Journal of Urology (in Japanese). 86 (5): 1044–1050. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.5980%2Fjpnjurol1989.86.1044">10.5980/jpnjurol1989.86.1044</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/7541089">7541089</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Nihon+Hinyokika+Gakkai+Zasshi.+The+Japanese+Journal+of+Urology&rft.atitle=%5BThe+preventive+effect+of+indeloxazine+hydrochloride+to+the+sexual+dysfunction+caused+by+anti-androgenergic+agent+%28allylestrenol%29%5D&rft.volume=86&rft.issue=5&rft.pages=1044-1050&rft.date=1995-05&rft_id=info%3Adoi%2F10.5980%2Fjpnjurol1989.86.1044&rft_id=info%3Apmid%2F7541089&rft.aulast=Horita&rft.aufirst=H&rft.au=Kumamoto%2C+Y&rft.au=Satoh%2C+Y&rft.au=Suzuki%2C+N&rft.au=Wada%2C+H&rft.au=Shibuya%2C+A&rft.au=Adachi%2C+H&rft.au=Kurohata%2C+T&rft.au=Tsukamoto%2C+T&rft_id=https%3A%2F%2Fdoi.org%2F10.5980%252Fjpnjurol1989.86.1044&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid9781436-40">^ <a href="#cite_ref-pmid9781436_40-0">a</a> <a href="#cite_ref-pmid9781436_40-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFNoguchiHaradaMasudaTakeda1998" class="citation journal cs1">Noguchi K, Harada M, Masuda M, Takeda M, Kinoshita Y, Fukushima S, et al. (September 1998). <a rel="nofollow" class="external text" href="https://doi.org/10.1111%2Fj.1442-2042.1998.tb00389.x">"Clinical significance of interruption of therapy with allylestrenol in patients with benign prostatic hypertrophy"</a>. International Journal of Urology. 5 (5): 466–470. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1111%2Fj.1442-2042.1998.tb00389.x">10.1111/j.1442-2042.1998.tb00389.x</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/9781436">9781436</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=International+Journal+of+Urology&rft.atitle=Clinical+significance+of+interruption+of+therapy+with+allylestrenol+in+patients+with+benign+prostatic+hypertrophy&rft.volume=5&rft.issue=5&rft.pages=466-470&rft.date=1998-09&rft_id=info%3Adoi%2F10.1111%2Fj.1442-2042.1998.tb00389.x&rft_id=info%3Apmid%2F9781436&rft.aulast=Noguchi&rft.aufirst=K&rft.au=Harada%2C+M&rft.au=Masuda%2C+M&rft.au=Takeda%2C+M&rft.au=Kinoshita%2C+Y&rft.au=Fukushima%2C+S&rft.au=Miyai%2C+K&rft.au=Fukuoka%2C+H&rft.au=Hosaka%2C+M&rft_id=https%3A%2F%2Fdoi.org%2F10.1111%252Fj.1442-2042.1998.tb00389.x&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid11107528-41"><a href="#cite_ref-pmid11107528_41-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFNoguchiUemuraTakedaSekiguchi2000" class="citation journal cs1 cs1-prop-foreign-lang-source">Noguchi K, Uemura H, Takeda M, Sekiguchi Y, Ogawa K, Hosaka M (September 2000). "[Rebound of prostate specific antigen after discontinuation of antiandrogen therapy for benign prostatic hyperplasia]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 46 (9): 605–607. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/11107528">11107528</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BRebound+of+prostate+specific+antigen+after+discontinuation+of+antiandrogen+therapy+for+benign+prostatic+hyperplasia%5D&rft.volume=46&rft.issue=9&rft.pages=605-607&rft.date=2000-09&rft_id=info%3Apmid%2F11107528&rft.aulast=Noguchi&rft.aufirst=K&rft.au=Uemura%2C+H&rft.au=Takeda%2C+M&rft.au=Sekiguchi%2C+Y&rft.au=Ogawa%2C+K&rft.au=Hosaka%2C+M&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid12094708-42"><a href="#cite_ref-pmid12094708_42-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFNoguchiTakedaHosakaKubota2002" class="citation journal cs1 cs1-prop-foreign-lang-source">Noguchi K, Takeda M, Hosaka M, Kubota Y (May 2002). "[Clinical effects of allylestrenol on patients with benign prostatic hyperplasia (BPH) evaluated with criteria for treatment efficacy in BPH]". Hinyokika Kiyo. Acta Urologica Japonica (in Japanese). 48 (5): 269–273. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/12094708">12094708</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=%5BClinical+effects+of+allylestrenol+on+patients+with+benign+prostatic+hyperplasia+%28BPH%29+evaluated+with+criteria+for+treatment+efficacy+in+BPH%5D&rft.volume=48&rft.issue=5&rft.pages=269-273&rft.date=2002-05&rft_id=info%3Apmid%2F12094708&rft.aulast=Noguchi&rft.aufirst=K&rft.au=Takeda%2C+M&rft.au=Hosaka%2C+M&rft.au=Kubota%2C+Y&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid16910584-43">^ <a href="#cite_ref-pmid16910584_43-0">a</a> <a href="#cite_ref-pmid16910584_43-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFNoguchiSuzukiTeranishiKondo2006" class="citation journal cs1">Noguchi K, Suzuki K, Teranishi J, Kondo K, Kishida T, Saito K, et al. (July 2006). "Recovery of serum prostate specific antigen value after interruption of antiandrogen therapy with allylestrenol for benign prostatic hyperplasia". Hinyokika Kiyo. Acta Urologica Japonica. 52 (7): 527–530. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/16910584">16910584</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Hinyokika+Kiyo.+Acta+Urologica+Japonica&rft.atitle=Recovery+of+serum+prostate+specific+antigen+value+after+interruption+of+antiandrogen+therapy+with+allylestrenol+for+benign+prostatic+hyperplasia&rft.volume=52&rft.issue=7&rft.pages=527-530&rft.date=2006-07&rft_id=info%3Apmid%2F16910584&rft.aulast=Noguchi&rft.aufirst=K&rft.au=Suzuki%2C+K&rft.au=Teranishi%2C+J&rft.au=Kondo%2C+K&rft.au=Kishida%2C+T&rft.au=Saito%2C+K&rft.au=Uemura%2C+H&rft.au=Kubota%2C+Y&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid6281750-44"><a href="#cite_ref-pmid6281750_44-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFTakeuchi1981" class="citation journal cs1">Takeuchi H (1981). "The therapeutic effect of concurrent administration of 5-fluorouracil and allylestrenol or hexestrol in small doses on prostatic carcinoma". The Prostate. Supplement. 1: 111–117. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2Fpros.2990020518">10.1002/pros.2990020518</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/6281750">6281750</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a> <a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:33940589">33940589</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=The+Prostate.+Supplement&rft.atitle=The+therapeutic+effect+of+concurrent+administration+of+5-fluorouracil+and+allylestrenol+or+hexestrol+in+small+doses+on+prostatic+carcinoma&rft.volume=1&rft.pages=111-117&rft.date=1981&rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A33940589%23id-name%3DS2CID&rft_id=info%3Apmid%2F6281750&rft_id=info%3Adoi%2F10.1002%2Fpros.2990020518&rft.aulast=Takeuchi&rft.aufirst=H&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid5057420-45"><a href="#cite_ref-pmid5057420_45-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFRiquelme_MorenoMontiel_LópezBravo_GuerraEscobar_Cauz1972" class="citation journal cs1 cs1-prop-foreign-lang-source">Riquelme Moreno E, Montiel López P, Bravo Guerra R, Escobar Cauz G (July 1972). "[Control of 5 cases of idiopathic precocious puberty with allylestrenol]". Ginecologia y Obstetricia de Mexico (in Spanish). 32 (189): 99–108. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/5057420">5057420</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Ginecologia+y+Obstetricia+de+Mexico&rft.atitle=%5BControl+of+5+cases+of+idiopathic+precocious+puberty+with+allylestrenol%5D&rft.volume=32&rft.issue=189&rft.pages=99-108&rft.date=1972-07&rft_id=info%3Apmid%2F5057420&rft.aulast=Riquelme+Moreno&rft.aufirst=E&rft.au=Montiel+L%C3%B3pez%2C+P&rft.au=Bravo+Guerra%2C+R&rft.au=Escobar+Cauz%2C+G&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Tripathi2013-46">^ <a href="#cite_ref-Tripathi2013_46-0">a</a> <a href="#cite_ref-Tripathi2013_46-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFTripathi2013" class="citation book cs1">Tripathi KD (30 September 2013). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=FfG8AQAAQBAJ&pg=PA318">Essentials of Medical Pharmacology</a>. JP Medical Ltd. pp. 318–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-93-5025-937-5" title="Special:BookSources/978-93-5025-937-5"><bdi>978-93-5025-937-5</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Essentials+of+Medical+Pharmacology&rft.pages=318-&rft.pub=JP+Medical+Ltd&rft.date=2013-09-30&rft.isbn=978-93-5025-937-5&rft.aulast=Tripathi&rft.aufirst=KD&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DFfG8AQAAQBAJ%26pg%3DPA318&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-SatoskarRege1973-47">^ <a href="#cite_ref-SatoskarRege1973_47-0">a</a> <a href="#cite_ref-SatoskarRege1973_47-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFSatoskarBhandarkarRege1973" class="citation book cs1">Satoskar RS, Bhandarkar SD, Rege NN (1973). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=7d493VOD4P8C&pg=PA941">"Gonadotropins, Estrogens, and Progesins"</a>. Pharmacology and Pharmacotherapeutics. Popular Prakashan. pp. 941–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-81-7991-527-1" title="Special:BookSources/978-81-7991-527-1"><bdi>978-81-7991-527-1</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=bookitem&rft.atitle=Gonadotropins%2C+Estrogens%2C+and+Progesins&rft.btitle=Pharmacology+and+Pharmacotherapeutics&rft.pages=941-&rft.pub=Popular+Prakashan&rft.date=1973&rft.isbn=978-81-7991-527-1&rft.aulast=Satoskar&rft.aufirst=RS&rft.au=Bhandarkar%2C+SD&rft.au=Rege%2C+NN&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3D7d493VOD4P8C%26pg%3DPA941&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-:1-48">^ <a href="#cite_ref-:1_48-0">a</a> <a href="#cite_ref-:1_48-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="https://www.drugs.com/aspirin.html">"Aspirin information from Drugs.com"</a>. <a rel="nofollow" class="external text" href="https://web.archive.org/web/20080509163105/http://www.drugs.com/aspirin.html">Archived</a> from the original on 9 May 2008. Retrieved 8 May 2008.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=Aspirin+information+from+Drugs.com&rft_id=https%3A%2F%2Fwww.drugs.com%2Faspirin.html&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-49"><a href="#cite_ref-49">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFRaithelBaenklerNaegelBuchwald2005" class="citation journal cs1">Raithel M, Baenkler HW, Naegel A, Buchwald F, Schultis HW, Backhaus B, et al. (September 2005). "Significance of salicylate intolerance in diseases of the lower gastrointestinal tract". Journal of Physiology and Pharmacology. 56 (Suppl 5): 89–102. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/16247191">16247191</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Journal+of+Physiology+and+Pharmacology&rft.atitle=Significance+of+salicylate+intolerance+in+diseases+of+the+lower+gastrointestinal+tract&rft.volume=56&rft.issue=Suppl+5&rft.pages=89-102&rft.date=2005-09&rft_id=info%3Apmid%2F16247191&rft.aulast=Raithel&rft.aufirst=M&rft.au=Baenkler%2C+HW&rft.au=Naegel%2C+A&rft.au=Buchwald%2C+F&rft.au=Schultis%2C+HW&rft.au=Backhaus%2C+B&rft.au=Kimpel%2C+S&rft.au=Koch%2C+H&rft.au=Mach%2C+K&rft.au=Hahn%2C+EG&rft.au=Konturek%2C+PC&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid7065053-50"><a href="#cite_ref-pmid7065053_50-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFRozenbaum1982" class="citation journal cs1">Rozenbaum H (March 1982). "Relationships between chemical structure and biological properties of progestogens". American Journal of Obstetrics and Gynecology. 142 (6 Pt 2): 719–724. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2FS0002-9378%2816%2932477-2">10.1016/S0002-9378(16)32477-2</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/7065053">7065053</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=American+Journal+of+Obstetrics+and+Gynecology&rft.atitle=Relationships+between+chemical+structure+and+biological+properties+of+progestogens&rft.volume=142&rft.issue=6+Pt+2&rft.pages=719-724&rft.date=1982-03&rft_id=info%3Adoi%2F10.1016%2FS0002-9378%2816%2932477-2&rft_id=info%3Apmid%2F7065053&rft.aulast=Rozenbaum&rft.aufirst=H&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid22078182-51">^ <a href="#cite_ref-pmid22078182_51-0">a</a> <a href="#cite_ref-pmid22078182_51-1">b</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFEndrikatGerlingerRichardRosenbaum2011" class="citation journal cs1">Endrikat J, Gerlinger C, Richard S, Rosenbaum P, Düsterberg B (December 2011). "Ovulation inhibition doses of progestins: a systematic review of the available literature and of marketed preparations worldwide". Contraception. 84 (6): 549–557. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.contraception.2011.04.009">10.1016/j.contraception.2011.04.009</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/22078182">22078182</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Contraception&rft.atitle=Ovulation+inhibition+doses+of+progestins%3A+a+systematic+review+of+the+available+literature+and+of+marketed+preparations+worldwide&rft.volume=84&rft.issue=6&rft.pages=549-557&rft.date=2011-12&rft_id=info%3Adoi%2F10.1016%2Fj.contraception.2011.04.009&rft_id=info%3Apmid%2F22078182&rft.aulast=Endrikat&rft.aufirst=J&rft.au=Gerlinger%2C+C&rft.au=Richard%2C+S&rft.au=Rosenbaum%2C+P&rft.au=D%C3%BCsterberg%2C+B&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Pincus2013-52"><a href="#cite_ref-Pincus2013_52-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFPincus2013" class="citation book cs1">Pincus G (3 September 2013). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=ehQlBQAAQBAJ&pg=PA222">The Control of Fertility</a>. Elsevier. pp. 222–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-1-4832-7088-3" title="Special:BookSources/978-1-4832-7088-3"><bdi>978-1-4832-7088-3</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=The+Control+of+Fertility&rft.pages=222-&rft.pub=Elsevier&rft.date=2013-09-03&rft.isbn=978-1-4832-7088-3&rft.aulast=Pincus&rft.aufirst=G&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DehQlBQAAQBAJ%26pg%3DPA222&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-LeidenbergerStrowitzki2009-53"><a href="#cite_ref-LeidenbergerStrowitzki2009_53-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFLeidenbergerStrowitzkiOrtmann2009" class="citation book cs1">Leidenberger FA, Strowitzki T, Ortmann O (29 August 2009). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=bqokBAAAQBAJ&pg=PA225">Klinische Endokrinologie für Frauenärzte</a>. Springer-Verlag. pp. 225–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-3-540-89760-6" title="Special:BookSources/978-3-540-89760-6"><bdi>978-3-540-89760-6</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Klinische+Endokrinologie+f%C3%BCr+Frauen%C3%A4rzte&rft.pages=225-&rft.pub=Springer-Verlag&rft.date=2009-08-29&rft.isbn=978-3-540-89760-6&rft.aulast=Leidenberger&rft.aufirst=FA&rft.au=Strowitzki%2C+T&rft.au=Ortmann%2C+O&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DbqokBAAAQBAJ%26pg%3DPA225&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid9268084-54">^ <a href="#cite_ref-pmid9268084_54-0">a</a> <a href="#cite_ref-pmid9268084_54-1">b</a> <a href="#cite_ref-pmid9268084_54-2">c</a> <a href="#cite_ref-pmid9268084_54-3">d</a> <a href="#cite_ref-pmid9268084_54-4">e</a> <a href="#cite_ref-pmid9268084_54-5">f</a> <a href="#cite_ref-pmid9268084_54-6">g</a> <a href="#cite_ref-pmid9268084_54-7">h</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFYasudaFujinoShirajiNambu1997" class="citation journal cs1">Yasuda N, Fujino K, Shiraji T, Nambu F, Kondo K (July 1997). <a rel="nofollow" class="external text" href="https://doi.org/10.1254%2Fjjp.74.243">"Effects of steroid 5alpha-reductase inhibitor ONO-9302 and anti-androgen allylestrenol on the prostatic growth, and plasma and prostatic hormone levels in rats"</a>. Japanese Journal of Pharmacology. 74 (3): 243–252. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1254%2Fjjp.74.243">10.1254/jjp.74.243</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/9268084">9268084</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Japanese+Journal+of+Pharmacology&rft.atitle=Effects+of+steroid+5alpha-reductase+inhibitor+ONO-9302+and+anti-androgen+allylestrenol+on+the+prostatic+growth%2C+and+plasma+and+prostatic+hormone+levels+in+rats&rft.volume=74&rft.issue=3&rft.pages=243-252&rft.date=1997-07&rft_id=info%3Adoi%2F10.1254%2Fjjp.74.243&rft_id=info%3Apmid%2F9268084&rft.aulast=Yasuda&rft.aufirst=N&rft.au=Fujino%2C+K&rft.au=Shiraji%2C+T&rft.au=Nambu%2C+F&rft.au=Kondo%2C+K&rft_id=https%3A%2F%2Fdoi.org%2F10.1254%252Fjjp.74.243&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid7000222-55"><a href="#cite_ref-pmid7000222_55-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFJacobiAltweinKurthBasting1980" class="citation journal cs1">Jacobi GH, Altwein JE, Kurth KH, Basting R, Hohenfellner R (June 1980). "Treatment of advanced prostatic cancer with parenteral cyproterone acetate: a phase III randomised trial". British Journal of Urology. 52 (3): 208–215. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1111%2Fj.1464-410X.1980.tb02961.x">10.1111/j.1464-410X.1980.tb02961.x</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/7000222">7000222</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=British+Journal+of+Urology&rft.atitle=Treatment+of+advanced+prostatic+cancer+with+parenteral+cyproterone+acetate%3A+a+phase+III+randomised+trial&rft.volume=52&rft.issue=3&rft.pages=208-215&rft.date=1980-06&rft_id=info%3Adoi%2F10.1111%2Fj.1464-410X.1980.tb02961.x&rft_id=info%3Apmid%2F7000222&rft.aulast=Jacobi&rft.aufirst=GH&rft.au=Altwein%2C+JE&rft.au=Kurth%2C+KH&rft.au=Basting%2C+R&rft.au=Hohenfellner%2C+R&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid6237116-56"><a href="#cite_ref-pmid6237116_56-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFKnuthHanoNieschlag1984" class="citation journal cs1">Knuth UA, Hano R, Nieschlag E (November 1984). "Effect of flutamide or cyproterone acetate on pituitary and testicular hormones in normal men". The Journal of Clinical Endocrinology and Metabolism. 59 (5): 963–969. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1210%2Fjcem-59-5-963">10.1210/jcem-59-5-963</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/6237116">6237116</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=The+Journal+of+Clinical+Endocrinology+and+Metabolism&rft.atitle=Effect+of+flutamide+or+cyproterone+acetate+on+pituitary+and+testicular+hormones+in+normal+men&rft.volume=59&rft.issue=5&rft.pages=963-969&rft.date=1984-11&rft_id=info%3Adoi%2F10.1210%2Fjcem-59-5-963&rft_id=info%3Apmid%2F6237116&rft.aulast=Knuth&rft.aufirst=UA&rft.au=Hano%2C+R&rft.au=Nieschlag%2C+E&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-pmid694436-57"><a href="#cite_ref-pmid694436_57-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFSanderNissen-MeyerAakvaag1978" class="citation journal cs1">Sander S, Nissen-Meyer R, Aakvaag A (1978). "On gestagen treatment of advanced prostatic carcinoma". Scandinavian Journal of Urology and Nephrology. 12 (2): 119–121. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.3109%2F00365597809179977">10.3109/00365597809179977</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/694436">694436</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Scandinavian+Journal+of+Urology+and+Nephrology&rft.atitle=On+gestagen+treatment+of+advanced+prostatic+carcinoma&rft.volume=12&rft.issue=2&rft.pages=119-121&rft.date=1978&rft_id=info%3Adoi%2F10.3109%2F00365597809179977&rft_id=info%3Apmid%2F694436&rft.aulast=Sander&rft.aufirst=S&rft.au=Nissen-Meyer%2C+R&rft.au=Aakvaag%2C+A&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Elks2014-58">^ <a href="#cite_ref-Elks2014_58-0">a</a> <a href="#cite_ref-Elks2014_58-1">b</a> <a href="#cite_ref-Elks2014_58-2">c</a> <a href="#cite_ref-Elks2014_58-3">d</a> <a href="#cite_ref-Elks2014_58-4">e</a> <a href="#cite_ref-Elks2014_58-5">f</a> <a href="#cite_ref-Elks2014_58-6">g</a> <a href="#cite_ref-Elks2014_58-7">h</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFElks2014" class="citation book cs1">Elks J (14 November 2014). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA31">The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies</a>. Springer. pp. 31–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-1-4757-2085-3" title="Special:BookSources/978-1-4757-2085-3"><bdi>978-1-4757-2085-3</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=The+Dictionary+of+Drugs%3A+Chemical+Data%3A+Chemical+Data%2C+Structures+and+Bibliographies&rft.pages=31-&rft.pub=Springer&rft.date=2014-11-14&rft.isbn=978-1-4757-2085-3&rft.aulast=Elks&rft.aufirst=J&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3D0vXTBwAAQBAJ%26pg%3DPA31&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-MVJain2017-59"><a href="#cite_ref-MVJain2017_59-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFAnitaSandhyaJainGoel2017" class="citation book cs1">Anita MV, Sandhya J, Jain, Goel N (31 December 2017). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=VrpEDwAAQBAJ&pg=PA10">Use of Progestogens in Clinical Practice of Obstetrics and Gynecology</a>. JP Medical Ltd. pp. 10–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-93-5270-218-3" title="Special:BookSources/978-93-5270-218-3"><bdi>978-93-5270-218-3</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Use+of+Progestogens+in+Clinical+Practice+of+Obstetrics+and+Gynecology&rft.pages=10-&rft.pub=JP+Medical+Ltd&rft.date=2017-12-31&rft.isbn=978-93-5270-218-3&rft.aulast=Anita&rft.aufirst=MV&rft.au=Sandhya%2C+J&rft.au=Jain&rft.au=Goel%2C+N&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DVrpEDwAAQBAJ%26pg%3DPA10&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Aronson2009-60">^ <a href="#cite_ref-Aronson2009_60-0">a</a> <a href="#cite_ref-Aronson2009_60-1">b</a> <a href="#cite_ref-Aronson2009_60-2">c</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFAronson2009" class="citation book cs1">Aronson JK (21 February 2009). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=BWMeSwVwfTkC&pg=PA289">Meyler's Side Effects of Endocrine and Metabolic Drugs</a>. Elsevier. pp. 289–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-0-08-093292-7" title="Special:BookSources/978-0-08-093292-7"><bdi>978-0-08-093292-7</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Meyler%27s+Side+Effects+of+Endocrine+and+Metabolic+Drugs&rft.pages=289-&rft.pub=Elsevier&rft.date=2009-02-21&rft.isbn=978-0-08-093292-7&rft.aulast=Aronson&rft.aufirst=JK&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DBWMeSwVwfTkC%26pg%3DPA289&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-GunnetDixon2000-61"><a href="#cite_ref-GunnetDixon2000_61-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFGunnetDixon2000" class="citation book cs1">Gunnet JW, Dixon LA (2000). "Hormones, Sex Hormones". Kirk-Othmer Encyclopedia of Chemical Technology. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2F0471238961.19052407211414.a01">10.1002/0471238961.19052407211414.a01</a>. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-0471238966" title="Special:BookSources/978-0471238966"><bdi>978-0471238966</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=bookitem&rft.atitle=Hormones%2C+Sex+Hormones&rft.btitle=Kirk-Othmer+Encyclopedia+of+Chemical+Technology&rft.date=2000&rft_id=info%3Adoi%2F10.1002%2F0471238961.19052407211414.a01&rft.isbn=978-0471238966&rft.aulast=Gunnet&rft.aufirst=JW&rft.au=Dixon%2C+LA&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-Springer2013-62"><a href="#cite_ref-Springer2013_62-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation book cs1"><a rel="nofollow" class="external text" href="https://books.google.com/books?id=t8GpBgAAQBAJ&pg=PA16">Die Gestagene</a>. Springer-Verlag. 27 November 2013. p. 16. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-3-642-99941-3" title="Special:BookSources/978-3-642-99941-3"><bdi>978-3-642-99941-3</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Die+Gestagene&rft.pages=16&rft.pub=Springer-Verlag&rft.date=2013-11-27&rft.isbn=978-3-642-99941-3&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3Dt8GpBgAAQBAJ%26pg%3DPA16&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-DeWinterSiegman1959-63"><a href="#cite_ref-DeWinterSiegman1959_63-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFDe_WinterSiegmanSzpilfogel1959" class="citation journal cs1">De Winter MS, Siegman CM, Szpilfogel SA (1959). "17-alkylated-3-deoxo-19-nor-testosterone". Chem. Ind.: 905.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Chem.+Ind.&rft.atitle=17-alkylated-3-deoxo-19-nor-testosterone&rft.pages=905&rft.date=1959&rft.aulast=De+Winter&rft.aufirst=MS&rft.au=Siegman%2C+CM&rft.au=Szpilfogel%2C+SA&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> <li id="cite_note-MortonHall2012-64"><a href="#cite_ref-MortonHall2012_64-0">^</a> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMortonHall2012" class="citation book cs1">Morton IK, Hall JM (6 December 2012). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=tsjrCAAAQBAJ&pg=PA11">Concise Dictionary of Pharmacological Agents: Properties and Synonyms</a>. Springer Science & Business Media. pp. 11–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-94-011-4439-1" title="Special:BookSources/978-94-011-4439-1"><bdi>978-94-011-4439-1</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Concise+Dictionary+of+Pharmacological+Agents%3A+Properties+and+Synonyms&rft.pages=11-&rft.pub=Springer+Science+%26+Business+Media&rft.date=2012-12-06&rft.isbn=978-94-011-4439-1&rft.aulast=Morton&rft.aufirst=IK&rft.au=Hall%2C+JM&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DtsjrCAAAQBAJ%26pg%3DPA11&rfr_id=info%3Asid%2Fen.wikipedia.org%3AAllylestrenol" class="Z3988"> </li> </ol></div></div> <div class="navbox-styles"><style data-mw-deduplicate="TemplateStyles:r1129693374">.mw-parser-output .hlist dl,.mw-parser-output .hlist ol,.mw-parser-output .hlist ul{margin:0;padding:0}.mw-parser-output .hlist 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.navbar{display:none!important}}</style><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Progestogens_and_antiprogestogens" title="Template:Progestogens and antiprogestogens"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Progestogens_and_antiprogestogens" title="Template talk:Progestogens and antiprogestogens"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Progestogens_and_antiprogestogens" title="Special:EditPage/Template:Progestogens and antiprogestogens"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Progestogens_and_antiprogestogens" style="font-size:114%;margin:0 4em"><a href="/wiki/Progestogen_(medication)" title="Progestogen (medication)">Progestogens</a> and <a href="/wiki/Antiprogestogen" title="Antiprogestogen">antiprogestogens</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;"><a href="/wiki/Progestogen_(medication)" title="Progestogen (medication)">Progestogens</a> (and <a href="/wiki/Progestin" class="mw-redirect" title="Progestin">progestins</a>)</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0;background:#DDDDFF;"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th id="PRTooltip_Progesterone_receptor_agonists" scope="row" class="navbox-group" style="width:8em;;text-align:center;"><a href="/wiki/Progesterone_receptor" title="Progesterone receptor"><abbr title="Progesterone receptor">PR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Progesterone receptor <a href="/wiki/Agonist" title="Agonist">agonists</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li>Progesterone derivatives: <a href="/wiki/Progesterone_(medication)" title="Progesterone (medication)">Progesterone</a></li> <li><a href="/wiki/Quingestrone" title="Quingestrone">Quingestrone</a></li></ul> <ul><li>Retroprogesterone derivatives: <a href="/wiki/Dydrogesterone" title="Dydrogesterone">Dydrogesterone</a></li> <li><a href="/wiki/Trengestone" title="Trengestone">Trengestone</a></li></ul> <ul><li>17α-Hydroxyprogesterone (and closely related) derivatives: 17α-Hydroxylated: <a href="/wiki/Acetomepregenol" title="Acetomepregenol">Acetomepregenol (mepregenol diacetate)</a></li> <li><a href="/wiki/Algestone_acetophenide" title="Algestone acetophenide">Algestone acetophenide (dihydroxyprogesterone acetophenide)</a></li> <li><a href="/wiki/Anagestone_acetate" title="Anagestone acetate">Anagestone acetate</a></li> <li><a href="/wiki/Chlormadinone_acetate" title="Chlormadinone acetate">Chlormadinone acetate</a></li> <li><a href="/wiki/Chlormethenmadinone_acetate" title="Chlormethenmadinone acetate">Chlormethenmadinone acetate</a></li> <li><a href="/wiki/Cyproterone_acetate" title="Cyproterone acetate">Cyproterone acetate</a></li> <li><a href="/wiki/Delmadinone_acetate" title="Delmadinone acetate">Delmadinone acetate</a></li> <li><a href="/wiki/Flugestone_acetate" title="Flugestone acetate">Flugestone acetate (flurogestone acetate)</a></li> <li><a href="/wiki/Flumedroxone_acetate" title="Flumedroxone acetate">Flumedroxone acetate</a></li> <li><a href="/wiki/Hydroxyprogesterone_acetate" title="Hydroxyprogesterone acetate">Hydroxyprogesterone acetate</a></li> <li><a href="/wiki/Hydroxyprogesterone_caproate" title="Hydroxyprogesterone caproate">Hydroxyprogesterone caproate</a></li> <li><a href="/wiki/Hydroxyprogesterone_heptanoate" title="Hydroxyprogesterone heptanoate">Hydroxyprogesterone heptanoate</a></li> <li><a href="/wiki/Medroxyprogesterone_acetate" title="Medroxyprogesterone acetate">Medroxyprogesterone acetate</a>#</li> <li><a href="/wiki/Megestrol_acetate" title="Megestrol acetate">Megestrol acetate</a></li> <li><a href="/wiki/Melengestrol_acetate" title="Melengestrol acetate">Melengestrol acetate</a></li> <li><a href="/wiki/Methenmadinone_acetate" title="Methenmadinone acetate">Methenmadinone acetate</a></li> <li><a href="/wiki/Osaterone_acetate" title="Osaterone acetate">Osaterone acetate</a></li> <li><a href="/wiki/Pentagestrone_acetate" title="Pentagestrone acetate">Pentagestrone acetate</a></li> <li><a href="/wiki/Proligestone" title="Proligestone">Proligestone</a>; 17α-Methylated: <a href="/wiki/Medrogestone" title="Medrogestone">Medrogestone</a>; Others: <a href="/wiki/Haloprogesterone" title="Haloprogesterone">Haloprogesterone</a></li></ul> <ul><li>19-Norprogesterone derivatives: 17α-Hydroxylated: <a href="/wiki/Gestonorone_caproate" title="Gestonorone caproate">Gestonorone caproate (gestronol hexanoate)</a></li> <li><a href="/wiki/Nomegestrol_acetate" title="Nomegestrol acetate">Nomegestrol acetate</a></li> <li><a href="/wiki/Norgestomet" title="Norgestomet">Norgestomet</a></li> <li><a href="/wiki/Segesterone_acetate" title="Segesterone acetate">Segesterone acetate (nestorone, elcometrine)</a>; 17α-Methylated: <a href="/wiki/Demegestone" title="Demegestone">Demegestone</a></li> <li><a href="/wiki/Promegestone" title="Promegestone">Promegestone</a></li> <li><a href="/wiki/Trimegestone" title="Trimegestone">Trimegestone</a></li></ul> <ul><li>Testosterone derivatives: Estranes: <a href="/wiki/Danazol" title="Danazol">Danazol</a></li> <li><a href="/wiki/Dimethisterone" title="Dimethisterone">Dimethisterone</a></li> <li><a href="/wiki/Ethisterone" title="Ethisterone">Ethisterone</a></li></ul> <ul><li>19-Nortestosterone derivatives: Estranes: <a class="mw-selflink selflink">Allylestrenol</a></li> <li><a href="/wiki/Altrenogest" title="Altrenogest">Altrenogest</a></li> <li><a href="/wiki/Dienogest" title="Dienogest">Dienogest</a></li> <li><a href="/wiki/Etynodiol_diacetate" title="Etynodiol diacetate">Etynodiol diacetate</a></li> <li><a href="/wiki/Lynestrenol" title="Lynestrenol">Lynestrenol</a></li> <li><a href="/wiki/Norethisterone" title="Norethisterone">Norethisterone (norethindrone)</a>#</li> <li><a href="/wiki/Norethisterone_acetate" title="Norethisterone acetate">Norethisterone acetate</a></li> <li><a href="/wiki/Norethisterone_enanthate" title="Norethisterone enanthate">Norethisterone enanthate</a></li> <li><a href="/wiki/Noretynodrel" title="Noretynodrel">Noretynodrel</a></li> <li><a href="/wiki/Norgesterone" title="Norgesterone">Norgesterone</a></li> <li><a href="/wiki/Norgestrienone" title="Norgestrienone">Norgestrienone</a></li> <li><a href="/wiki/Normethandrone" title="Normethandrone">Normethandrone (methylestrenolone)</a></li> <li><a href="/wiki/Norvinisterone" title="Norvinisterone">Norvinisterone</a></li> <li><a href="/wiki/Oxendolone" title="Oxendolone">Oxendolone</a></li> <li><a href="/wiki/Quingestanol_acetate" title="Quingestanol acetate">Quingestanol acetate</a></li> <li><a href="/wiki/Tibolone" title="Tibolone">Tibolone</a>; Gonanes: <a href="/wiki/Desogestrel" title="Desogestrel">Desogestrel</a></li> <li><a href="/wiki/Etonogestrel" title="Etonogestrel">Etonogestrel</a></li> <li><a href="/wiki/Gestodene" title="Gestodene">Gestodene</a></li> <li><a href="/wiki/Gestrinone" title="Gestrinone">Gestrinone</a></li> <li><a href="/wiki/Levonorgestrel" title="Levonorgestrel">Levonorgestrel</a>#</li> <li><a href="/wiki/Norelgestromin" title="Norelgestromin">Norelgestromin</a></li> <li><a href="/wiki/Norgestimate" title="Norgestimate">Norgestimate</a></li> <li><a href="/wiki/Norgestrel" title="Norgestrel">Norgestrel</a></li></ul> <ul><li>Spirolactone derivatives: <a href="/wiki/Drospirenone" title="Drospirenone">Drospirenone</a></li></ul> <ul><li>Others: <a href="/wiki/Anabolic%E2%80%93androgenic_steroid" class="mw-redirect" title="Anabolic–androgenic steroid">Anabolic–androgenic steroids</a> (e.g., <a href="/wiki/Nandrolone" title="Nandrolone">nandrolone</a> and <a href="/wiki/Nandrolone_ester" class="mw-redirect" title="Nandrolone ester">esters</a>, <a href="/wiki/Trenbolone" title="Trenbolone">trenbolone</a> and <a href="/wiki/Trenbolone_ester" class="mw-redirect" title="Trenbolone ester">esters</a>, <a href="/wiki/Ethylestrenol" title="Ethylestrenol">ethylestrenol</a>, <a href="/wiki/Norethandrolone" title="Norethandrolone">norethandrolone</a>, others)</li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;"><a href="/wiki/Antiprogestogen" title="Antiprogestogen">Antiprogestogens</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0;background:#DDDDFF;"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:8em;;text-align:center;"><a href="/wiki/Selective_progesterone_receptor_modulators" class="mw-redirect" title="Selective progesterone receptor modulators"><abbr title="Selective progesterone receptor modulators">SPRMs</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Selective progesterone receptor modulators</th><td class="navbox-list-with-group navbox-list navbox-even" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Telapristone" title="Telapristone">Telapristone</a>§</li> <li><a href="/wiki/Ulipristal_acetate" title="Ulipristal acetate">Ulipristal acetate</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:8em;;text-align:center;"><a href="/wiki/Progesterone_receptor" title="Progesterone receptor"><abbr title="Progesterone receptor">PR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Progesterone receptor <a href="/wiki/Receptor_antagonist" title="Receptor antagonist">antagonists</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Aglepristone" title="Aglepristone">Aglepristone</a></li> <li><a href="/wiki/Mifepristone" title="Mifepristone">Mifepristone</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><td colspan="2" class="navbox-list navbox-even hlist" style="width:100%;padding:0;background:#DDDDFF;"><div style="padding:0 0.25em"><div class="hlist"> <ul><li>#<a href="/wiki/WHO_Model_List_of_Essential_Medicines" title="WHO Model List of Essential Medicines">WHO-EM</a></li> <li>‡<a href="/wiki/List_of_withdrawn_drugs" title="List of withdrawn drugs">Withdrawn</a> from market</li> <li><a href="/wiki/Clinical_trial" title="Clinical trial">Clinical trials</a>: <ul><li>†<a href="/wiki/Phases_of_clinical_research#Phase_III" title="Phases of clinical research">Phase III</a></li> <li>§Never to phase III</li></ul></li></ul> </div> <dl><dt>See also</dt> <dd><a href="/wiki/Template:Progesterone_receptor_modulators" title="Template:Progesterone receptor modulators">Progesterone receptor modulators</a></dd> <dd><a href="/wiki/Template:Androgens_and_antiandrogens" title="Template:Androgens and antiandrogens">Androgens and antiandrogens</a></dd> <dd><a href="/wiki/Template:Estrogens_and_antiestrogens" title="Template:Estrogens and antiestrogens">Estrogens and antiestrogens</a></dd> <dd><a href="/wiki/List_of_steroidal_progestogens" class="mw-redirect" title="List of steroidal progestogens">List of progestogens</a></dd></dl></div></td></tr></tbody></table></div> <div class="navbox-styles"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1236075235"></div><div role="navigation" class="navbox" aria-labelledby="Drugs_used_in_benign_prostatic_hyperplasia_(G04C)" style="padding:3px"><table class="nowraplinks mw-collapsible mw-collapsed navbox-inner" style="border-spacing:0;background:transparent;color:inherit"><tbody><tr><th scope="col" class="navbox-title" colspan="2"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1239400231"><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Drugs_used_in_benign_prostatic_hypertrophy" title="Template:Drugs used in benign prostatic hypertrophy"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Drugs_used_in_benign_prostatic_hypertrophy" title="Template talk:Drugs used in benign prostatic hypertrophy"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Drugs_used_in_benign_prostatic_hypertrophy" title="Special:EditPage/Template:Drugs used in benign prostatic hypertrophy"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Drugs_used_in_benign_prostatic_hyperplasia_(G04C)" style="font-size:114%;margin:0 4em">Drugs used in <a href="/wiki/Benign_prostatic_hyperplasia" title="Benign prostatic hyperplasia">benign prostatic hyperplasia</a> (<a href="/wiki/ATC_code_G04#G04C" title="ATC code G04">G04C</a>)</div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/5%CE%B1-Reductase_inhibitor" title="5α-Reductase inhibitor">5α-Reductase inhibitors</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Dutasteride" title="Dutasteride">Dutasteride</a></li> <li><a href="/wiki/Epristeride" title="Epristeride">Epristeride</a></li> <li><a href="/wiki/Finasteride" title="Finasteride">Finasteride</a> (<a href="/wiki/Finasteride/tadalafil" title="Finasteride/tadalafil">+tadalafil</a>)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Alpha-1_blocker" title="Alpha-1 blocker">Alpha-1 blockers</a></th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Alfuzosin" title="Alfuzosin">Alfuzosin</a></li> <li><a href="/wiki/Doxazosin" title="Doxazosin">Doxazosin</a></li> <li><a href="/wiki/Silodosin" title="Silodosin">Silodosin</a></li> <li><a href="/wiki/Tamsulosin" title="Tamsulosin">Tamsulosin</a></li> <li><a href="/wiki/Terazosin" title="Terazosin">Terazosin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Steroidal_antiandrogen" title="Steroidal antiandrogen">Steroidal antiandrogens</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a class="mw-selflink selflink">Allylestrenol</a></li> <li><a href="/wiki/Delmadinone_acetate" title="Delmadinone acetate">Delmadinone acetate</a></li> <li><a href="/wiki/Gestonorone_caproate" title="Gestonorone caproate">Gestonorone caproate</a></li> <li><a href="/wiki/Osaterone_acetate" title="Osaterone acetate">Osaterone acetate</a></li> <li><a href="/wiki/Oxendolone" title="Oxendolone">Oxendolone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Herbal_medicine" title="Herbal medicine">Herbal products</a></th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Pygeum_(herbal_remedy)" class="mw-redirect" title="Pygeum (herbal remedy)">Pygeum africanum</a></li> <li><a href="/wiki/Saw_palmetto_extract" title="Saw palmetto extract">Saw palmetto extract</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Others</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Mepartricin" title="Mepartricin">Mepartricin</a></li></ul> </div></td></tr></tbody></table></div> <div class="navbox-styles"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1236075235"></div><div role="navigation" class="navbox" aria-labelledby="Progesterone_receptor_modulators" style="padding:3px"><table class="nowraplinks hlist mw-collapsible mw-collapsed navbox-inner" style="border-spacing:0;background:transparent;color:inherit"><tbody><tr><th scope="col" class="navbox-title" colspan="2"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1239400231"><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Progesterone_receptor_modulators" title="Template:Progesterone receptor modulators"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Progesterone_receptor_modulators" title="Template talk:Progesterone receptor modulators"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Progesterone_receptor_modulators" title="Special:EditPage/Template:Progesterone receptor modulators"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Progesterone_receptor_modulators" style="font-size:114%;margin:0 4em"><a href="/wiki/Progesterone_receptor" title="Progesterone receptor">Progesterone receptor</a> <a href="/wiki/Receptor_modulator" title="Receptor modulator">modulators</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;"><a href="/wiki/Progesterone_receptor" title="Progesterone receptor"><abbr title="Progesterone receptor">PR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Progesterone receptor</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:6em;;text-align:center">Agonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li>Progesterone derivatives: <a href="/wiki/3%CE%B2-Dihydroprogesterone" title="3β-Dihydroprogesterone">3β-Dihydroprogesterone</a></li> <li><a href="/wiki/5%CE%B1-Dihydroprogesterone" title="5α-Dihydroprogesterone">5α-Dihydroprogesterone</a></li> <li><a href="/wiki/6%CE%B1-Methylprogesterone" title="6α-Methylprogesterone">6α-Methylprogesterone</a></li> <li><a href="/wiki/9%CE%B1-Bromo-11-ketoprogesterone" class="mw-redirect" title="9α-Bromo-11-ketoprogesterone">9α-Bromo-11-ketoprogesterone</a></li> <li><a href="/wiki/11-Dehydroprogesterone" title="11-Dehydroprogesterone">11-Dehydroprogesterone</a></li> <li><a href="/wiki/11-Deoxycorticosterone" title="11-Deoxycorticosterone">11-Deoxycorticosterone</a></li> <li><a href="/wiki/16%CE%B1-Hydroxyprogesterone" title="16α-Hydroxyprogesterone">16α-Hydroxyprogesterone</a></li> <li><a href="/w/index.php?title=17%CE%B1-Methyl-11-deoxycorticosterone_acetate&action=edit&redlink=1" class="new" title="17α-Methyl-11-deoxycorticosterone acetate (page does not exist)">17α-Methyl-11-deoxycorticosterone acetate</a></li> <li><a href="/wiki/20%CE%B1-Dihydroprogesterone" title="20α-Dihydroprogesterone">20α-Dihydroprogesterone</a></li> <li><a href="/wiki/20%CE%B2-Dihydroprogesterone" title="20β-Dihydroprogesterone">20β-Dihydroprogesterone</a></li> <li><a href="/wiki/Dimepregnen" title="Dimepregnen">Dimepregnen</a></li> <li><a href="/wiki/Diosgenin" title="Diosgenin">Diosgenin</a></li> <li><a href="/wiki/P1-185" title="P1-185">P1-185</a></li> <li><a href="/wiki/Progesterone" title="Progesterone">Progesterone</a></li> <li><a href="/wiki/Progesterone_3-acetyl_enol_ether" title="Progesterone 3-acetyl enol ether">Progesterone 3-acetyl enol ether</a></li> <li><a href="/wiki/Quingestrone" title="Quingestrone">Quingestrone</a></li></ul> <ul><li>Retroprogesterone derivatives: <a href="/wiki/20%CE%B1-Dihydrodydrogesterone" title="20α-Dihydrodydrogesterone">20α-Dihydrodydrogesterone</a></li> <li><a href="/wiki/20%CE%B1-Dihydrotrengestone" title="20α-Dihydrotrengestone">20α-Dihydrotrengestone</a></li> <li><a href="/wiki/DU-41164" title="DU-41164">DU-41164</a></li> <li><a href="/wiki/DU-41165" title="DU-41165">DU-41165</a></li> <li><a href="/wiki/Dydrogesterone" title="Dydrogesterone">Dydrogesterone</a></li> <li><a href="/wiki/Retroprogesterone" title="Retroprogesterone">Retroprogesterone</a></li> <li><a href="/wiki/Ro_6-3129" title="Ro 6-3129">Ro 6-3129</a></li> <li><a href="/wiki/Trengestone" title="Trengestone">Trengestone</a></li></ul> <ul><li>17α-Substituted progesterone derivatives: <a href="/wiki/6%CE%B1-Methyl-17%CE%B1-bromoprogesterone" title="6α-Methyl-17α-bromoprogesterone">6α-Methyl-17α-bromoprogesterone</a></li> <li><a href="/wiki/15%CE%B2-Hydroxycyproterone_acetate" title="15β-Hydroxycyproterone acetate">15β-Hydroxycyproterone acetate</a></li> <li><a href="/wiki/16-Methylene-17%CE%B1-hydroxyprogesterone_acetate" title="16-Methylene-17α-hydroxyprogesterone acetate">16-Methylene-17α-hydroxyprogesterone acetate</a></li> <li><a href="/wiki/17%CE%B1-Bromoprogesterone" title="17α-Bromoprogesterone">17α-Bromoprogesterone</a></li> <li><a href="/wiki/17%CE%B1-Hydroxyprogesterone" title="17α-Hydroxyprogesterone">17α-Hydroxyprogesterone (hydroxyprogesterone)</a></li> <li><a href="/wiki/17%CE%B1-Methylprogesterone" title="17α-Methylprogesterone">17α-Methylprogesterone</a></li> <li><a href="/wiki/Acetomepregenol" title="Acetomepregenol">Acetomepregenol (mepregenol diacetate)</a></li> <li><a href="/wiki/Algestone" title="Algestone">Algestone</a></li> <li><a href="/wiki/Algestone_acetonide" title="Algestone acetonide">Algestone acetonide</a></li> <li><a href="/wiki/Algestone_acetophenide" title="Algestone acetophenide">Algestone acetophenide</a></li> <li><a href="/wiki/Anagestone" title="Anagestone">Anagestone</a></li> <li><a href="/wiki/Anagestone_acetate" title="Anagestone acetate">Anagestone acetate</a></li> <li><a href="/w/index.php?title=Bromethenmadinone&action=edit&redlink=1" class="new" title="Bromethenmadinone (page does not exist)">Bromethenmadinone</a></li> <li><a href="/wiki/Bromethenmadinone_acetate" title="Bromethenmadinone acetate">Bromethenmadinone acetate</a></li> <li><a href="/wiki/Butagest" title="Butagest">Butagest (buterol)</a></li> <li><a href="/wiki/Chlormadinone" title="Chlormadinone">Chlormadinone</a></li> <li><a href="/wiki/Chlormadinone_acetate" title="Chlormadinone acetate">Chlormadinone acetate</a></li> <li><a href="/wiki/Chlormadinone_caproate" title="Chlormadinone caproate">Chlormadinone caproate</a></li> <li><a href="/w/index.php?title=Chlormethenmadinone&action=edit&redlink=1" class="new" title="Chlormethenmadinone (page does not exist)">Chlormethenmadinone</a></li> <li><a href="/wiki/Chlormethenmadinone_acetate" title="Chlormethenmadinone acetate">Chlormethenmadinone acetate</a></li> <li><a href="/wiki/Cismadinone" title="Cismadinone">Cismadinone</a></li> <li><a href="/wiki/Cismadinone_acetate" title="Cismadinone acetate">Cismadinone acetate</a></li> <li><a href="/wiki/Clogestone" title="Clogestone">Clogestone</a></li> <li><a href="/wiki/Clogestone_acetate" title="Clogestone acetate">Clogestone acetate</a></li> <li><a href="/wiki/Clomegestone" title="Clomegestone">Clomegestone</a></li> <li><a href="/wiki/Clomegestone_acetate" title="Clomegestone acetate">Clomegestone acetate</a></li> <li><a href="/wiki/Cymegesolate" title="Cymegesolate">Cymegesolate</a></li> <li><a href="/wiki/Cyproterone_acetate" title="Cyproterone acetate">Cyproterone acetate</a></li> <li><a href="/wiki/Delmadinone" title="Delmadinone">Delmadinone</a></li> <li><a href="/wiki/Delmadinone_acetate" title="Delmadinone acetate">Delmadinone acetate</a></li> <li><a href="/wiki/Edogestrone" title="Edogestrone">Edogestrone</a></li> <li><a href="/wiki/Flugestone" title="Flugestone">Flugestone</a></li> <li><a href="/wiki/Flugestone_acetate" title="Flugestone acetate">Flugestone acetate</a></li> <li><a href="/wiki/Fluorometholone" title="Fluorometholone">Fluorometholone</a></li> <li><a href="/wiki/Fluorometholone_acetate" title="Fluorometholone acetate">Fluorometholone acetate</a></li> <li><a href="/wiki/Flumedroxone" title="Flumedroxone">Flumedroxone</a></li> <li><a href="/wiki/Flumedroxone_acetate" title="Flumedroxone acetate">Flumedroxone acetate</a></li> <li><a href="/wiki/Fluoromedroxyprogesterone_acetate" title="Fluoromedroxyprogesterone acetate">Fluoromedroxyprogesterone acetate</a></li> <li><a href="/wiki/Gestaclone" title="Gestaclone">Gestaclone</a></li> <li><a href="/w/index.php?title=Gestobutanoyl&action=edit&redlink=1" class="new" title="Gestobutanoyl (page does not exist)">Gestobutanoyl</a></li> <li><a href="/wiki/Haloprogesterone" title="Haloprogesterone">Haloprogesterone</a></li> <li><a href="/wiki/Hydromadinone" title="Hydromadinone">Hydromadinone</a></li> <li><a href="/wiki/Hydromadinone_acetate" title="Hydromadinone acetate">Hydromadinone acetate</a></li> <li><a href="/wiki/Hydroxyprogesterone_acetate" title="Hydroxyprogesterone acetate">Hydroxyprogesterone acetate</a></li> <li><a href="/wiki/Hydroxyprogesterone_caproate" title="Hydroxyprogesterone caproate">Hydroxyprogesterone caproate (hydroxyprogesterone hexanoate)</a></li> <li><a href="/wiki/Hydroxyprogesterone_heptanoate" title="Hydroxyprogesterone heptanoate">Hydroxyprogesterone heptanoate (hydroxyprogesterone enanthate)</a></li> <li><a href="/wiki/Hydroxyprogesterone_heptanoate_benzilic_acid_hydrazone" title="Hydroxyprogesterone heptanoate benzilic acid hydrazone">Hydroxyprogesterone heptanoate benzilic acid hydrazone</a></li> <li><a href="/wiki/Mecigestone" title="Mecigestone">Mecigestone (pentarane B)</a></li> <li><a href="/wiki/Medrogestone" title="Medrogestone">Medrogestone</a></li> <li><a href="/wiki/Medroxyprogesterone" title="Medroxyprogesterone">Medroxyprogesterone</a></li> <li><a href="/wiki/Medroxyprogesterone_acetate" title="Medroxyprogesterone acetate">Medroxyprogesterone acetate</a></li> <li><a href="/wiki/Medroxyprogesterone_caproate" title="Medroxyprogesterone caproate">Medroxyprogesterone caproate</a></li> <li><a href="/wiki/Megestrol" title="Megestrol">Megestrol</a></li> <li><a href="/wiki/Megestrol_acetate" title="Megestrol acetate">Megestrol acetate</a></li> <li><a href="/wiki/Megestrol_caproate" title="Megestrol caproate">Megestrol caproate</a></li> <li><a href="/wiki/Melengestrol" title="Melengestrol">Melengestrol</a></li> <li><a href="/wiki/Melengestrol_acetate" title="Melengestrol acetate">Melengestrol acetate</a></li> <li><a href="/wiki/Methenmadinone" title="Methenmadinone">Methenmadinone</a></li> <li><a href="/wiki/Methenmadinone_acetate" title="Methenmadinone acetate">Methenmadinone acetate</a></li> <li><a href="/wiki/Methenmadinone_caproate" title="Methenmadinone caproate">Methenmadinone caproate</a></li> <li><a href="/wiki/Mometasone" title="Mometasone">Mometasone</a></li> <li><a href="/wiki/Mometasone_furoate" class="mw-redirect" title="Mometasone furoate">Mometasone furoate</a></li> <li><a href="/wiki/Osaterone" title="Osaterone">Osaterone</a></li> <li><a href="/wiki/Osaterone_acetate" title="Osaterone acetate">Osaterone acetate</a></li> <li><a href="/wiki/Pentagestrone" title="Pentagestrone">Pentagestrone</a></li> <li><a href="/wiki/Pentagestrone_acetate" title="Pentagestrone acetate">Pentagestrone acetate</a></li> <li><a href="/wiki/Pentarane_A" title="Pentarane A">Pentarane A</a></li> <li><a href="/wiki/Proligestone" title="Proligestone">Proligestone</a></li> <li><a href="/wiki/Triamcinolone_acetonide" title="Triamcinolone acetonide">Triamcinolone acetonide</a></li></ul> <ul><li>19-Norprogesterone derivatives: <a href="/wiki/17%CE%B1-Methyl-19-norprogesterone" title="17α-Methyl-19-norprogesterone">17α-Methyl-19-norprogesterone</a></li> <li><a href="/wiki/18-Methylsegesterone_acetate" title="18-Methylsegesterone acetate">18-Methylsegesterone acetate</a></li> <li><a href="/wiki/19-Norprogesterone" title="19-Norprogesterone">19-Norprogesterone</a></li> <li><a href="/wiki/Amadinone" title="Amadinone">Amadinone</a></li> <li><a href="/wiki/Amadinone_acetate" title="Amadinone acetate">Amadinone acetate</a></li> <li><a href="/wiki/Demegestone" title="Demegestone">Demegestone</a></li> <li><a href="/w/index.php?title=Fluoro_ethyl_norprogesterone&action=edit&redlink=1" class="new" title="Fluoro ethyl norprogesterone (page does not exist)">Fluoro ethyl norprogesterone</a></li> <li><a href="/w/index.php?title=Fluoro_furanyl_norprogesterone&action=edit&redlink=1" class="new" title="Fluoro furanyl norprogesterone (page does not exist)">Fluoro furanyl norprogesterone</a></li> <li><a href="/wiki/Gestadienol" title="Gestadienol">Gestadienol</a></li> <li><a href="/wiki/Gestadienol_acetate" title="Gestadienol acetate">Gestadienol acetate</a></li> <li><a href="/wiki/Gestonorone_acetate" title="Gestonorone acetate">Gestonorone acetate (gestronol acetate)</a></li> <li><a href="/wiki/Gestonorone_caproate" title="Gestonorone caproate">Gestonorone caproate (gestronol hexanoate)</a></li> <li><a href="/wiki/Gestronol" title="Gestronol">Gestronol (gestonorone)</a></li> <li><a href="/wiki/Nomegestrol" title="Nomegestrol">Nomegestrol</a></li> <li><a href="/wiki/Nomegestrol_acetate" title="Nomegestrol acetate">Nomegestrol acetate</a></li> <li><a href="/wiki/Norgestomet" title="Norgestomet">Norgestomet</a></li> <li><a href="/wiki/ORG-2058" title="ORG-2058">ORG-2058</a></li> <li><a href="/wiki/Oxogestone" title="Oxogestone">Oxogestone</a></li> <li><a href="/wiki/Oxogestone_phenpropionate" title="Oxogestone phenpropionate">Oxogestone phenpropionate (xinogestone)</a></li> <li><a href="/wiki/Promegestone" title="Promegestone">Promegestone</a></li> <li><a href="/wiki/Segesterone" title="Segesterone">Segesterone</a></li> <li><a href="/wiki/Nestorone" class="mw-redirect" title="Nestorone">Segesterone acetate (nestorone)</a></li> <li><a href="/wiki/Trimegestone" title="Trimegestone">Trimegestone</a></li></ul> <ul><li>Testosterone derivatives: Progestins: <a href="/wiki/6,6-Difluoronorethisterone" title="6,6-Difluoronorethisterone">6,6-Difluoronorethisterone</a></li> <li><a href="/wiki/6,6-Difluoronorethisterone_acetate" title="6,6-Difluoronorethisterone acetate">6,6-Difluoronorethisterone acetate</a></li> <li><a href="/wiki/17%CE%B1-Allyl-19-nortestosterone" title="17α-Allyl-19-nortestosterone">17α-Allyl-19-nortestosterone</a></li> <li><a class="mw-selflink selflink">Allylestrenol</a></li> <li><a href="/wiki/Altrenogest" title="Altrenogest">Altrenogest</a></li> <li><a href="/wiki/Chloroethynylnorgestrel" title="Chloroethynylnorgestrel">Chloroethynylnorgestrel</a></li> <li><a href="/wiki/Cingestol" title="Cingestol">Cingestol</a></li> <li><a href="/wiki/Danazol" title="Danazol">Danazol</a></li> <li><a href="/wiki/Desogestrel" title="Desogestrel">Desogestrel</a></li> <li><a href="/wiki/Dienogest" title="Dienogest">Dienogest</a></li> <li><a href="/wiki/Ethinylandrostenediol" title="Ethinylandrostenediol">Ethinylandrostenediol</a> <ul><li><a href="/wiki/Ethandrostate" title="Ethandrostate">Ethandrostate</a></li></ul></li> <li><a href="/wiki/Ethisterone" title="Ethisterone">Ethisterone</a></li> <li><a href="/wiki/Ethynerone" title="Ethynerone">Ethynerone</a></li> <li><a href="/wiki/Etonogestrel" title="Etonogestrel">Etonogestrel</a></li> <li><a href="/wiki/Etynodiol" title="Etynodiol">Etynodiol</a></li> <li><a href="/wiki/Etynodiol_diacetate" title="Etynodiol diacetate">Etynodiol diacetate</a></li> <li><a href="/wiki/Gestodene" title="Gestodene">Gestodene</a></li> <li><a href="/wiki/Gestrinone" title="Gestrinone">Gestrinone</a></li> <li><a href="/wiki/Levonorgestrel" title="Levonorgestrel">Levonorgestrel</a></li> <li><a href="/wiki/Levonorgestrel_ester" class="mw-redirect" title="Levonorgestrel ester">Levonorgestrel esters</a> (e.g., <a href="/wiki/Levonorgestrel_butanoate" title="Levonorgestrel butanoate">levonorgestrel butanoate</a>)</li> <li><a href="/wiki/Lynestrenol" title="Lynestrenol">Lynestrenol</a></li> <li><a href="/wiki/Lynestrenol_phenylpropionate" title="Lynestrenol phenylpropionate">Lynestrenol phenylpropionate</a></li> <li><a href="/wiki/Metynodiol" title="Metynodiol">Metynodiol</a></li> <li><a href="/wiki/Metynodiol_diacetate" title="Metynodiol diacetate">Metynodiol diacetate</a></li> <li><a href="/wiki/Norelgestromin" title="Norelgestromin">Norelgestromin</a></li> <li><a href="/wiki/Norethisterone" title="Norethisterone">Norethisterone (norethindrone)</a></li> <li><a href="/wiki/Norethisterone_ester" class="mw-redirect" title="Norethisterone ester">Norethisterone esters</a> (e.g., <a href="/wiki/Norethisterone_acetate" title="Norethisterone acetate">norethisterone acetate</a>, <a href="/wiki/Norethisterone_enanthate" title="Norethisterone enanthate">norethisterone enanthate</a>)</li> <li><a href="/wiki/Noretynodrel" title="Noretynodrel">Noretynodrel</a></li> <li><a href="/wiki/Norgesterone" title="Norgesterone">Norgesterone</a></li> <li><a href="/wiki/Norgestimate" title="Norgestimate">Norgestimate</a></li> <li><a href="/wiki/Norgestrel" title="Norgestrel">Norgestrel</a></li> <li><a href="/wiki/Norgestrienone" title="Norgestrienone">Norgestrienone</a></li> <li><a href="/wiki/Norvinisterone" title="Norvinisterone">Norvinisterone</a></li> <li><a href="/wiki/Oxendolone" title="Oxendolone">Oxendolone</a></li> <li><a href="/wiki/Quingestanol" title="Quingestanol">Quingestanol</a></li> <li><a href="/wiki/Quingestanol_acetate" title="Quingestanol acetate">Quingestanol acetate</a></li> <li><a href="/wiki/Tibolone" title="Tibolone">Tibolone</a></li> <li><a href="/wiki/Tigestol" title="Tigestol">Tigestol</a></li> <li><a href="/wiki/Tosagestin" title="Tosagestin">Tosagestin</a>; Anabolic–androgenic steroids: <a href="/wiki/11%CE%B2-Methyl-19-nortestosterone" title="11β-Methyl-19-nortestosterone">11β-Methyl-19-nortestosterone</a></li> <li><a href="/wiki/11%CE%B2-Methyl-19-nortestosterone_dodecylcarbonate" title="11β-Methyl-19-nortestosterone dodecylcarbonate">11β-Methyl-19-nortestosterone dodecylcarbonate</a></li> <li><a href="/wiki/19-Nor-5-androstenediol" title="19-Nor-5-androstenediol">19-Nor-5-androstenediol</a></li> <li><a href="/wiki/19-Nor-5-androstenedione" title="19-Nor-5-androstenedione">19-Nor-5-androstenedione</a></li> <li><a href="/wiki/19-Nordehydroepiandrosterone" title="19-Nordehydroepiandrosterone">19-Nordehydroepiandrosterone</a></li> <li><a href="/wiki/Bolandiol" title="Bolandiol">Bolandiol</a></li> <li><a href="/wiki/Bolandiol_dipropionate" title="Bolandiol dipropionate">Bolandiol dipropionate</a></li> <li><a href="/wiki/Bolandione" title="Bolandione">Bolandione</a></li> <li><a href="/wiki/Dimethisterone" title="Dimethisterone">Dimethisterone</a></li> <li><a href="/wiki/Dienedione" title="Dienedione">Dienedione</a></li> <li><a href="/wiki/Dienolone" title="Dienolone">Dienolone</a></li> <li><a href="/wiki/Dimethandrolone" title="Dimethandrolone">Dimethandrolone</a></li> <li><a href="/wiki/Dimethandrolone_buciclate" title="Dimethandrolone buciclate">Dimethandrolone buciclate</a></li> <li><a href="/wiki/Dimethandrolone_dodecylcarbonate" title="Dimethandrolone dodecylcarbonate">Dimethandrolone dodecylcarbonate</a></li> <li><a href="/wiki/Dimethandrolone_undecanoate" title="Dimethandrolone undecanoate">Dimethandrolone undecanoate</a></li> <li><a href="/wiki/Dimethyldienolone" title="Dimethyldienolone">Dimethyldienolone</a></li> <li><a href="/wiki/Dimethyltrienolone" title="Dimethyltrienolone">Dimethyltrienolone</a></li> <li><a href="/wiki/Ethyldienolone" title="Ethyldienolone">Ethyldienolone</a></li> <li><a href="/wiki/Ethylestrenol" title="Ethylestrenol">Ethylestrenol (ethylnandrol)</a></li> <li><a href="/wiki/Methyldienolone" title="Methyldienolone">Methyldienolone</a></li> <li><a href="/wiki/Metribolone" title="Metribolone">Metribolone (R-1881)</a></li> <li><a href="/wiki/Methoxydienone" title="Methoxydienone">Methoxydienone (methoxygonadiene)</a></li> <li><a href="/wiki/Mibolerone" title="Mibolerone">Mibolerone</a></li> <li><a href="/wiki/Nandrolone" title="Nandrolone">Nandrolone</a></li> <li><a href="/wiki/Nandrolone_ester" class="mw-redirect" title="Nandrolone ester">Nandrolone esters</a> (e.g., <a href="/wiki/Nandrolone_decanoate" title="Nandrolone decanoate">nandrolone decanoate</a>, <a href="/wiki/Nandrolone_phenylpropionate" title="Nandrolone phenylpropionate">nandrolone phenylpropionate</a>)</li> <li><a href="/wiki/Norethandrolone" title="Norethandrolone">Norethandrolone</a></li> <li><a href="/wiki/Normethandrone" title="Normethandrone">Normethandrone (methylestrenolone, normethandrolone, normethisterone)</a></li> <li><a href="/wiki/RU-2309" title="RU-2309">RU-2309</a></li> <li><a href="/wiki/Tetrahydrogestrinone" title="Tetrahydrogestrinone">Tetrahydrogestrinone</a></li> <li><a href="/wiki/Trenbolone" title="Trenbolone">Trenbolone (trienolone)</a></li> <li><a href="/wiki/Trenbolone_ester" class="mw-redirect" title="Trenbolone ester">Trenbolone esters</a> (e.g., <a href="/wiki/Trenbolone_acetate" title="Trenbolone acetate">trenbolone acetate</a>, <a href="/wiki/Trenbolone_enanthate" title="Trenbolone enanthate">trenbolone enanthate</a>)</li> <li><a href="/wiki/Trendione" title="Trendione">Trendione</a></li> <li><a href="/wiki/Trestolone" title="Trestolone">Trestolone</a></li> <li><a href="/wiki/Trestolone_acetate" title="Trestolone acetate">Trestolone acetate</a></li></ul> <ul><li>Spirolactone derivatives: <a href="/wiki/Canrenoic_acid" title="Canrenoic acid">Canrenoic acid</a></li> <li><a href="/wiki/Canrenone" title="Canrenone">Canrenone</a></li> <li><a href="/wiki/Drospirenone" title="Drospirenone">Drospirenone</a></li> <li><a href="/wiki/Mespirenone" title="Mespirenone">Mespirenone</a></li> <li><a href="/wiki/Potassium_canrenoate" title="Potassium canrenoate">Potassium canrenoate</a></li> <li><a href="/wiki/Prorenone" title="Prorenone">Prorenone</a></li> <li><a href="/wiki/SC-5233" title="SC-5233">SC-5233 (spirolactone)</a></li> <li><a href="/wiki/SC-8109" title="SC-8109">SC-8109</a></li> <li><a href="/wiki/Spironolactone" title="Spironolactone">Spironolactone</a></li> <li><a href="/wiki/Spirorenone" title="Spirorenone">Spirorenone</a></li></ul> <ul><li>Nonsteroidal: <a href="/wiki/3,8-Dihydrodiligustilide" title="3,8-Dihydrodiligustilide">3,8-Dihydrodiligustilide</a></li> <li><a href="/wiki/LG-2527" title="LG-2527">LG-2527</a></li> <li><a href="/w/index.php?title=LG-100128&action=edit&redlink=1" class="new" title="LG-100128 (page does not exist)">LG-100128</a></li> <li><a href="/wiki/Riligustilide" title="Riligustilide">Riligustilide</a></li> <li><a href="/w/index.php?title=RWJ-26819&action=edit&redlink=1" class="new" title="RWJ-26819 (page does not exist)">RWJ-26819</a></li> <li><a href="/w/index.php?title=RWJ-49853&action=edit&redlink=1" class="new" title="RWJ-49853 (page does not exist)">RWJ-49853</a></li> <li><a href="/w/index.php?title=RWJ-60130&action=edit&redlink=1" class="new" title="RWJ-60130 (page does not exist)">RWJ-60130</a></li> <li><a href="/wiki/Tanaproget" title="Tanaproget">Tanaproget</a></li> <li><a href="/wiki/ZM-182345" title="ZM-182345">ZM-182345</a></li></ul> <ul><li>Unknown: <a href="/wiki/ORG-47241" title="ORG-47241">ORG-47241</a></li> <li><a href="/wiki/ORG-201745" title="ORG-201745">ORG-201745</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:6em;;text-align:center">Mixed (<a href="/wiki/Selective_progesterone_receptor_modulators" class="mw-redirect" title="Selective progesterone receptor modulators"><abbr title="Selective progesterone receptor modulators">SPRMs</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Selective progesterone receptor modulators)</th><td class="navbox-list-with-group navbox-list navbox-even" style="padding:0"><div style="padding:0 0.25em"> <ul><li>Steroidal: <a href="/wiki/Dihydroethisterone" class="mw-redirect" title="Dihydroethisterone">Dihydroethisterone</a></li> <li><a href="/wiki/5%CE%B1-Dihydrolevonorgestrel" title="5α-Dihydrolevonorgestrel">5α-Dihydrolevonorgestrel</a></li> <li><a href="/wiki/5%CE%B1-Dihydronorethisterone" title="5α-Dihydronorethisterone">5α-Dihydronorethisterone</a></li> <li><a href="/wiki/Asoprisnil" title="Asoprisnil">Asoprisnil</a></li> <li><a href="/wiki/Asoprisnil_ecamate" title="Asoprisnil ecamate">Asoprisnil ecamate</a></li> <li><a href="/wiki/Guggulsterone" title="Guggulsterone">Guggulsterone</a></li> <li><a href="/w/index.php?title=J1042&action=edit&redlink=1" class="new" title="J1042 (page does not exist)">J1042</a></li> <li><a href="/w/index.php?title=LG-120838&action=edit&redlink=1" class="new" title="LG-120838 (page does not exist)">LG-120838</a></li> <li><a href="/wiki/Metapristone" title="Metapristone">Metapristone (RU-42633)</a></li> <li><a href="/wiki/Mifepristone" title="Mifepristone">Mifepristone (RU-486)</a></li> <li><a href="/w/index.php?title=ORF-9371&action=edit&redlink=1" class="new" title="ORF-9371 (page does not exist)">ORF-9371</a></li> <li><a href="/wiki/ORF-9326" class="mw-redirect" title="ORF-9326">ORF-9326</a></li> <li><a href="/w/index.php?title=ORG-31710&action=edit&redlink=1" class="new" title="ORG-31710 (page does not exist)">ORG-31710</a></li> <li><a href="/w/index.php?title=ORG-33628&action=edit&redlink=1" class="new" title="ORG-33628 (page does not exist)">ORG-33628</a></li> <li><a href="/w/index.php?title=RMI-12936&action=edit&redlink=1" class="new" title="RMI-12936 (page does not exist)">RMI-12936</a></li> <li><a href="/wiki/Telapristone" title="Telapristone">Telapristone</a></li> <li><a href="/wiki/Ulipristal_acetate" title="Ulipristal acetate">Ulipristal acetate</a></li> <li><a href="/wiki/Vilaprisan" title="Vilaprisan">Vilaprisan</a></li> <li><a href="/w/index.php?title=ZK-137316&action=edit&redlink=1" class="new" title="ZK-137316 (page does not exist)">ZK-137316</a></li></ul> <ul><li>Nonsteroidal: <a href="/wiki/Apigenin" title="Apigenin">Apigenin</a></li> <li><a href="/wiki/Kaempferol" title="Kaempferol">Kaempferol</a></li> <li><a href="/w/index.php?title=LG-120920&action=edit&redlink=1" class="new" title="LG-120920 (page does not exist)">LG-120920</a></li> <li><a href="/wiki/Naringenin" title="Naringenin">Naringenin</a></li> <li><a href="/w/index.php?title=PRA-910&action=edit&redlink=1" class="new" title="PRA-910 (page does not exist)">PRA-910</a></li> <li><a href="/wiki/Syringic_acid" title="Syringic acid">Syringic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:6em;;text-align:center">Antagonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li>Steroidal: <a href="/wiki/Aglepristone" title="Aglepristone">Aglepristone</a></li> <li><a href="/wiki/Lilopristone" title="Lilopristone">Lilopristone</a></li> <li><a href="/wiki/Lonaprisan" title="Lonaprisan">Lonaprisan</a></li> <li><a href="/wiki/Onapristone" title="Onapristone">Onapristone</a></li> <li><a href="/w/index.php?title=ORG-31710&action=edit&redlink=1" class="new" title="ORG-31710 (page does not exist)">ORG-31710</a></li> <li><a href="/w/index.php?title=ORG-31806&action=edit&redlink=1" class="new" title="ORG-31806 (page does not exist)">ORG-31806</a></li> <li><a href="/w/index.php?title=ORG-33628&action=edit&redlink=1" class="new" title="ORG-33628 (page does not exist)">ORG-33628</a></li> <li><a href="/w/index.php?title=RTI_3021%E2%80%93022&action=edit&redlink=1" class="new" title="RTI 3021–022 (page does not exist)">RTI 3021–022</a></li> <li><a href="/wiki/Toripristone" title="Toripristone">Toripristone</a></li> <li><a href="/wiki/Zanoterone" title="Zanoterone">Zanoterone</a></li></ul> <ul><li>Nonsteroidal: <a href="/wiki/Darolutamide" title="Darolutamide">Darolutamide</a></li> <li><a href="/w/index.php?title=LG-001447&action=edit&redlink=1" class="new" title="LG-001447 (page does not exist)">LG-001447</a></li> <li><a href="/w/index.php?title=LG-100127&action=edit&redlink=1" class="new" title="LG-100127 (page does not exist)">LG-100127</a></li> <li><a href="/w/index.php?title=LG-100128&action=edit&redlink=1" class="new" title="LG-100128 (page does not exist)">LG-100128</a></li> <li><a href="/w/index.php?title=LG-120830&action=edit&redlink=1" class="new" title="LG-120830 (page does not exist)">LG-120830</a></li> <li><a href="/w/index.php?title=LG-121046&action=edit&redlink=1" class="new" title="LG-121046 (page does not exist)">LG-121046</a></li> <li><a href="/wiki/Valproic_acid" class="mw-redirect" title="Valproic acid">Valproic acid</a></li> <li><a href="/w/index.php?title=ZM-150271&action=edit&redlink=1" class="new" title="ZM-150271 (page does not exist)">ZM-150271</a></li> <li><a href="/w/index.php?title=ZM-172406&action=edit&redlink=1" class="new" title="ZM-172406 (page does not exist)">ZM-172406</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;"><a href="/wiki/Membrane_progesterone_receptor" title="Membrane progesterone receptor"><abbr title="Membrane progesterone receptor">mPR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Membrane progesterone receptor (<a href="/wiki/Progestin_and_adipoQ_receptor" title="Progestin and adipoQ receptor"><abbr title="Progestin and adipoQ receptor">PAQR</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Progestin and adipoQ receptor)</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:6em;;text-align:center">Agonists</th><td class="navbox-list-with-group navbox-list navbox-even" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/5%CE%B1-Dihydroprogesterone" title="5α-Dihydroprogesterone">5α-Dihydroprogesterone</a></li> <li><a href="/wiki/5%CE%B2-Dihydroprogesterone" title="5β-Dihydroprogesterone">5β-Dihydroprogesterone</a></li> <li><a href="/wiki/11-Deoxycorticosterone" title="11-Deoxycorticosterone">11-Deoxycortisone (21-hydroxyprogesterone)</a></li> <li><a href="/wiki/11-Deoxycortisol" title="11-Deoxycortisol">11-Deoxycortisol (17α,21-dihydroxyprogesterone)</a></li> <li><a href="/wiki/17%CE%B1-Hydroxyprogesterone" title="17α-Hydroxyprogesterone">17α-Hydroxyprogesterone</a></li> <li><a href="/wiki/Allopregnanolone" title="Allopregnanolone">Allopregnanolone</a></li> <li><a href="/wiki/Mifepristone" title="Mifepristone">Mifepristone</a></li> <li><a href="/wiki/Pregnenolone" title="Pregnenolone">Pregnenolone</a></li> <li><a href="/wiki/Progesterone" title="Progesterone">Progesterone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:6em;;text-align:center">Antagonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Mifepristone" title="Mifepristone">Mifepristone</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><td class="navbox-abovebelow" colspan="2"><div> <dl><dt>See also</dt> <dd><a href="/wiki/Template:Receptor_modulators" title="Template:Receptor modulators">Receptor/signaling modulators</a></dd> <dd><a href="/wiki/Template:Progestogens_and_antiprogestogens" title="Template:Progestogens and antiprogestogens">Progestogens and antiprogestogens</a></dd> <dd><a href="/wiki/Template:Androgen_receptor_modulators" title="Template:Androgen receptor modulators">Androgen receptor modulators</a></dd> <dd><a href="/wiki/Template:Estrogen_receptor_modulators" title="Template:Estrogen receptor modulators">Estrogen receptor modulators</a></dd> <dd><a href="/wiki/List_of_steroidal_progestogens" class="mw-redirect" title="List of steroidal progestogens">List of progestogens</a></dd></dl> </div></td></tr></tbody></table></div>    </div><noscript><img src="https://login.wikimedia.org/wiki/Special:CentralAutoLogin/start?type=1x1" alt="" width="1" height="1" style="border: none; position: absolute;"></noscript> 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