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Cilnidipine: Difference between revisions - Wikipedia
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Available in 7 languages" > <label id="p-lang-btn-label" for="p-lang-btn-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--action-progressive mw-portlet-lang-heading-7" aria-hidden="true" ><span class="vector-icon mw-ui-icon-language-progressive mw-ui-icon-wikimedia-language-progressive"></span> <span class="vector-dropdown-label-text">7 languages</span> </label> <div class="vector-dropdown-content"> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li class="interlanguage-link interwiki-es mw-list-item"><a href="https://es.wikipedia.org/wiki/Cilnidipino" title="Cilnidipino – Spanish" lang="es" hreflang="es" data-title="Cilnidipino" data-language-autonym="Español" data-language-local-name="Spanish" class="interlanguage-link-target"><span>Español</span></a></li><li class="interlanguage-link interwiki-fa mw-list-item"><a href="https://fa.wikipedia.org/wiki/%D8%B3%DB%8C%D9%84%D9%86%DB%8C%D8%AF%DB%8C%D9%BE%DB%8C%D9%86" title="سیلنیدیپین – Persian" lang="fa" hreflang="fa" data-title="سیلنیدیپین" data-language-autonym="فارسی" data-language-local-name="Persian" class="interlanguage-link-target"><span>فارسی</span></a></li><li class="interlanguage-link interwiki-hu mw-list-item"><a href="https://hu.wikipedia.org/wiki/Cilnidipin" title="Cilnidipin – Hungarian" lang="hu" hreflang="hu" data-title="Cilnidipin" data-language-autonym="Magyar" data-language-local-name="Hungarian" class="interlanguage-link-target"><span>Magyar</span></a></li><li class="interlanguage-link interwiki-ja mw-list-item"><a href="https://ja.wikipedia.org/wiki/%E3%82%B7%E3%83%AB%E3%83%8B%E3%82%B8%E3%83%94%E3%83%B3" title="シルニジピン – Japanese" lang="ja" hreflang="ja" data-title="シルニジピン" data-language-autonym="日本語" data-language-local-name="Japanese" class="interlanguage-link-target"><span>日本語</span></a></li><li class="interlanguage-link interwiki-pl mw-list-item"><a href="https://pl.wikipedia.org/wiki/Cylnidypina" title="Cylnidypina – Polish" lang="pl" hreflang="pl" data-title="Cylnidypina" data-language-autonym="Polski" data-language-local-name="Polish" class="interlanguage-link-target"><span>Polski</span></a></li><li class="interlanguage-link interwiki-sr mw-list-item"><a href="https://sr.wikipedia.org/wiki/Cilnidipin" title="Cilnidipin – Serbian" lang="sr" hreflang="sr" data-title="Cilnidipin" data-language-autonym="Српски / srpski" data-language-local-name="Serbian" class="interlanguage-link-target"><span>Српски / srpski</span></a></li><li class="interlanguage-link interwiki-sh mw-list-item"><a href="https://sh.wikipedia.org/wiki/Cilnidipin" title="Cilnidipin – Serbo-Croatian" lang="sh" hreflang="sh" data-title="Cilnidipin" data-language-autonym="Srpskohrvatski / српскохрватски" data-language-local-name="Serbo-Croatian" class="interlanguage-link-target"><span>Srpskohrvatski / српскохрватски</span></a></li> </ul> 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class="minoredit" title="This is a minor edit">m</abbr> <span class="comment comment--without-parentheses">added details on ongoing study program in Australia for Systemic Sclerosis and Raynaud's</span></div><div id="mw-diff-otitle5"></div><div id="mw-diff-otitle4"><a href="/w/index.php?title=Cilnidipine&diff=prev&oldid=1113276731" title="Cilnidipine" id="differences-prevlink">← Previous edit</a></div></td> <td colspan="2" class="diff-ntitle diff-side-added"><div id="mw-diff-ntitle1"><strong><a href="/w/index.php?title=Cilnidipine&oldid=1248419281" title="Cilnidipine">Revision as of 11:59, 29 September 2024</a> <span class="mw-diff-edit"><a href="/w/index.php?title=Cilnidipine&action=edit&oldid=1248419281" title="Cilnidipine">edit</a></span><span class="mw-diff-timestamp" data-timestamp="2024-09-29T11:59:19Z"></span> <span class="mw-diff-undo"><a href="/w/index.php?title=Cilnidipine&action=edit&undoafter=1113276731&undo=1248419281" title=""Undo" reverts this edit and opens the edit 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It allows adding a reason in the summary.">undo</a></span></strong></div><div id="mw-diff-ntitle2"><a href="/wiki/User:JWBE" class="mw-userlink" title="User:JWBE" data-mw-revid="1248419281"><bdi>JWBE</bdi></a> <span class="mw-usertoollinks">(<a href="/wiki/User_talk:JWBE" class="mw-usertoollinks-talk" title="User talk:JWBE">talk</a> | <a href="/wiki/Special:Contributions/JWBE" class="mw-usertoollinks-contribs" title="Special:Contributions/JWBE">contribs</a>)</span><div class="mw-diff-usermetadata"><div class="mw-diff-userroles"><a href="/wiki/Wikipedia:Extended_confirmed_editors" class="mw-redirect" title="Wikipedia:Extended confirmed editors">Extended confirmed users</a></div><div class="mw-diff-usereditcount"><span>10,111</span> edits</div></div></div><div id="mw-diff-ntitle3"> <span class="comment comment--without-parentheses">removed <a href="/wiki/Category:Nitrobenzene_derivatives" title="Category:Nitrobenzene derivatives">Category:Nitrobenzene derivatives</a>; added <a href="/wiki/Category:3-Nitrophenyl_compounds" title="Category:3-Nitrophenyl compounds">Category:3-Nitrophenyl compounds</a> using <a href="/wiki/Wikipedia:HC" class="mw-redirect" title="Wikipedia:HC">HotCat</a></span></div><div id="mw-diff-ntitle5"></div><div id="mw-diff-ntitle4"><a href="/w/index.php?title=Cilnidipine&diff=next&oldid=1248419281" title="Cilnidipine" id="differences-nextlink">Next edit →</a></div></td> </tr><tr><td colspan="4" class="diff-multi" lang="en">(12 intermediate revisions by 10 users not shown)</td></tr><tr> <td colspan="2" class="diff-lineno">Line 1:</td> <td colspan="2" class="diff-lineno">Line 1:</td> </tr> <tr> <td colspan="2" class="diff-empty diff-side-deleted"></td> <td class="diff-marker" data-marker="+"></td> <td class="diff-addedline diff-side-added"><div>{{short description|Antihypertensive drug of the calcium channel blocker class}}</div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>{{Drugbox</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>{{Drugbox</div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>| IUPAC_name = 3-(''E'')-3-Phenyl-2-propenyl 5-2-methoxyethyl 2,6-dimethyl-4-(''m''-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>| IUPAC_name = 3-(''E'')-3-Phenyl-2-propenyl 5-2-methoxyethyl 2,6-dimethyl-4-(''m''-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate</div></td> </tr> <tr> <td colspan="2" class="diff-lineno">Line 42:</td> <td colspan="2" class="diff-lineno">Line 43:</td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>}}</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>}}</div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div><!-- Definition and medical uses --></div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div><!-- Definition and medical uses --></div></td> </tr> <tr> <td class="diff-marker" data-marker="−"></td> <td class="diff-deletedline diff-side-deleted"><div>'''Cilnidipine''' is a [[calcium channel blocker]]. Cilnidipine is approved for use in Japan, China, India, Nepal, and Korea<del class="diffchange diffchange-inline">.</del> [[hypertension]]. </div></td> <td class="diff-marker" data-marker="+"></td> <td class="diff-addedline diff-side-added"><div>'''Cilnidipine''' is a [[calcium channel blocker]]. Cilnidipine is approved for use in Japan, China, India, Nepal, and Korea<ins class="diffchange diffchange-inline"> for</ins> [[hypertension]]. </div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><br /></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><br /></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div><!-- Side effects and mechanisms --></div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div><!-- Side effects and mechanisms --></div></td> </tr> <tr> <td colspan="2" class="diff-lineno">Line 53:</td> <td colspan="2" class="diff-lineno">Line 54:</td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>Cilnidipine decreases blood pressure and is used to treat hypertension and its [[Comorbidity|comorbidities]]. Due to its blocking action at the <small>N</small>-type and <small>L</small>-type calcium channel, cilnidipine dilates both [[arteriole]]s and [[venule]]s, reducing the pressure in the [[capillary bed]]. Cilnidipine is vasoselective and has a weak direct [[dromotropic]] effect, a strong vasodepressor effect, and an arrhythmia-inhibiting effect.</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>Cilnidipine decreases blood pressure and is used to treat hypertension and its [[Comorbidity|comorbidities]]. Due to its blocking action at the <small>N</small>-type and <small>L</small>-type calcium channel, cilnidipine dilates both [[arteriole]]s and [[venule]]s, reducing the pressure in the [[capillary bed]]. Cilnidipine is vasoselective and has a weak direct [[dromotropic]] effect, a strong vasodepressor effect, and an arrhythmia-inhibiting effect.</div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>Blood pressure control with cilnidipine treatment in Japanese post-stroke hypertensive patients [The CA-ATTEND study] - the results of a large-scale prospective post-marketing surveillance study of post-stroke hypertensive patients (n = 2667, male 60.4%, 69.0 ± 10.9 years) treated with cilnidipine indicate that cilnidipine was effective in treating uncontrolled blood pressure and was well tolerated in post-stroke hypertensive patients.<ref>{{cite journal | vauthors = Aoki S, Hosomi N, Nezu T, Teshima T, Sugii H, Nagahama S, Kurose Y, Maruyama H, Matsumoto M | display-authors = 6 | title = Blood pressure control with cilnidipine treatment in Japanese post-stroke hypertensive patients: The CA-ATTEND study | journal = Clinical and Experimental Hypertension | volume = 39 | issue = 3 | pages = 225–234 | year = 2017 | pmid = 28448181 | doi = 10.1080/10641963.2016.1235183 | doi-access = free }}</ref></div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>Blood pressure control with cilnidipine treatment in Japanese post-stroke hypertensive patients [The CA-ATTEND study] - the results of a large-scale prospective post-marketing surveillance study of post-stroke hypertensive patients (n = 2667, male 60.4%, 69.0 ± 10.9 years) treated with cilnidipine indicate that cilnidipine was effective in treating uncontrolled blood pressure and was well tolerated in post-stroke hypertensive patients.<ref>{{cite journal | vauthors = Aoki S, Hosomi N, Nezu T, Teshima T, Sugii H, Nagahama S, Kurose Y, Maruyama H, Matsumoto M | display-authors = 6 | title = Blood pressure control with cilnidipine treatment in Japanese post-stroke hypertensive patients: The CA-ATTEND study | journal = Clinical and Experimental Hypertension | volume = 39 | issue = 3 | pages = 225–234 | year = 2017 | pmid = 28448181 | doi = 10.1080/10641963.2016.1235183 | doi-access = free }}</ref></div></td> </tr> <tr> <td class="diff-marker" data-marker="−"></td> <td class="diff-deletedline diff-side-deleted"><div>The Ambulatory Blood Pressure Control and Home Blood Pressure (Morning and Evening) Lowering By N-Channel Blocker Cilnidipine (ACHIEVE-ONE) trial is a large-scale (n=2319) clinical study on blood pressure (BP) and pulse rate (PR) in the real world with use of cilnidipine - this study revealed that Cilnidipine significantly reduced BP and PR in hypertensive patients at the clinic and at home, especially with higher BP and PR in the morning. Cilnidipine is currently being studied in the RECONNOITER study in Australia for its effect on Raynaud's and other manifestations of disease in patients with Systemic Sclerosis. <ref>{{cite journal | vauthors = Kario K, Ando S, Kido H, Nariyama J, Takiuchi S, Yagi T, Shimizu T, Eguchi K, Ohno M, Kinoshita O, Yamada T | display-authors = 6 | title = The effects of the L/N-type calcium channel blocker (cilnidipine) on sympathetic hyperactive morning hypertension: results from ACHIEVE-ONE | journal = Journal of Clinical Hypertension | volume = 15 | issue = 2 | pages = 133–42 | date = February 2013 | pmid = 23339732 | doi = 10.1111/jch.12042 }}</ref></div></td> <td class="diff-marker" data-marker="+"></td> <td class="diff-addedline diff-side-added"><div>The Ambulatory Blood Pressure Control and Home Blood Pressure (Morning and Evening) Lowering By N-Channel Blocker Cilnidipine (ACHIEVE-ONE) trial is a large-scale (n=2319) clinical study on blood pressure (BP) and pulse rate (PR) in the real world with use of cilnidipine - this study revealed that Cilnidipine significantly reduced BP and PR in hypertensive patients at the clinic and at home, especially with higher BP and PR in the morning. Cilnidipine is currently being studied in the RECONNOITER study in Australia for its effect on Raynaud's and other manifestations of disease in patients with Systemic Sclerosis. <ref>{{cite journal | vauthors = Kario K, Ando S, Kido H, Nariyama J, Takiuchi S, Yagi T, Shimizu T, Eguchi K, Ohno M, Kinoshita O, Yamada T | display-authors = 6 | title = The effects of the L/N-type calcium channel blocker (cilnidipine) on sympathetic hyperactive morning hypertension: results from ACHIEVE-ONE | journal = Journal of Clinical Hypertension | volume = 15 | issue = 2 | pages = 133–42 | date = February 2013 | pmid = 23339732 | doi = 10.1111/jch.12042<ins class="diffchange diffchange-inline"> | pmc = 8034443 }}</ref><ref>{{cite web | url=https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=380810&isReview=true | title=ANZCTR - Registration</ins> }}</ref></div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><br /></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><br /></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>== Side effects ==</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>== Side effects ==</div></td> </tr> <tr> <td colspan="2" class="diff-lineno">Line 61:</td> <td colspan="2" class="diff-lineno">Line 62:</td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><br /></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><br /></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>== Brand Name ==</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>== Brand Name ==</div></td> </tr> <tr> <td class="diff-marker" data-marker="−"></td> <td class="diff-deletedline diff-side-deleted"><div>In India, it is sold under the brand name cilacar, clinblue, among others at doses of 5mg/10mg/20mg.<ref>{{cite web | url=https://medicaldialogues.in/partner/jbcpl/cilacar-cilnidipine | title=Cilacar (Cilnidipine): Uses, Side Effects, Dosage - Medical Dialogues | publisher=[[Medical Dialogues]] | date=3 March 2021 | access-date=3 March 2021}}</ref></div></td> <td class="diff-marker" data-marker="+"></td> <td class="diff-addedline diff-side-added"><div>In India, it is sold under the brand name<ins class="diffchange diffchange-inline"> Cinod,</ins> cilacar, clinblue, among others at doses of 5mg/10mg/20mg.<ref>{{cite web | url=https://medicaldialogues.in/partner/jbcpl/cilacar-cilnidipine | title=Cilacar (Cilnidipine): Uses, Side Effects, Dosage - Medical Dialogues | publisher=[[Medical Dialogues]] | date=3 March 2021 | access-date=3 March 2021}}</ref></div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><br /></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><br /></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>==History==</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>==History==</div></td> </tr> <tr> <td colspan="2" class="diff-lineno">Line 74:</td> <td colspan="2" class="diff-lineno">Line 75:</td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>{{refend}}</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>{{refend}}</div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><br /></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><br /></td> </tr> <tr> <td class="diff-marker" data-marker="−"></td> <td class="diff-deletedline diff-side-deleted"><div>[[Category:Aldosterone synthase inhibitors]]</div></td> <td colspan="2" class="diff-empty diff-side-added"></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>[[Category:Calcium channel blockers]]</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>[[Category:Calcium channel blockers]]</div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>[[Category:Dihydropyridines]]</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>[[Category:Dihydropyridines]]</div></td> </tr> <tr> <td class="diff-marker" data-marker="−"></td> <td class="diff-deletedline diff-side-deleted"><div>[[Category:<del class="diffchange diffchange-inline">Nitro</del> compounds]]</div></td> <td class="diff-marker" data-marker="+"></td> <td class="diff-addedline diff-side-added"><div>[[Category:<ins class="diffchange diffchange-inline">3-Nitrophenyl</ins> compounds]]</div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>[[Category:Carboxylate esters]]</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>[[Category:Carboxylate esters]]</div></td> </tr> <tr> <td class="diff-marker"></td> <td class="diff-context diff-side-deleted"><div>[[Category:Ethers]]</div></td> <td class="diff-marker"></td> <td class="diff-context diff-side-added"><div>[[Category:Ethers]]</div></td> </tr> </table><hr class='diff-hr' id='mw-oldid' /> <h2 class='diff-currentversion-title'>Revision as of 11:59, 29 September 2024</h2> <div class="mw-content-ltr mw-parser-output" lang="en" dir="ltr"><div class="shortdescription nomobile noexcerpt noprint searchaux" style="display:none">Antihypertensive drug of the calcium channel blocker class</div> <div class="shortdescription nomobile noexcerpt noprint searchaux" style="display:none">Pharmaceutical 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"><span title="International nonproprietary name (INN): Cilnidipine">Cilnidipine</span></caption><tbody><tr><td colspan="2" class="infobox-image notheme" style="background-color: #f8f9fa;"><span typeof="mw:File"><a href="/wiki/File:Cilnidipine.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/75/Cilnidipine.svg/250px-Cilnidipine.svg.png" decoding="async" width="250" height="132" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/75/Cilnidipine.svg/375px-Cilnidipine.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/75/Cilnidipine.svg/500px-Cilnidipine.svg.png 2x" data-file-width="512" data-file-height="271" /></a></span></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">Atelec (アテレック), Cilaheart, Cilacar</td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/American_Society_of_Health-System_Pharmacists" title="American Society of Health-System Pharmacists">AHFS</a>/<a href="/wiki/Drugs.com" title="Drugs.com">Drugs.com</a></th><td class="infobox-data"><span title="www.drugs.com"><a rel="nofollow" class="external text" href="https://www.drugs.com/international/cilnidipine.html">International Drug Names</a></span></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"><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><a href="/wiki/ATC_code_C08" title="ATC code C08">C08CA14</a> (<span title="www.whocc.no"><a rel="nofollow" class="external text" href="https://www.whocc.no/atc_ddd_index/?code=C08CA14">WHO</a></span>) </li></ul></div></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%;">3-(<i>E</i>)-3-Phenyl-2-propenyl 5-2-methoxyethyl 2,6-dimethyl-4-(<i>m</i>-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate</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><span title="commonchemistry.cas.org"><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=132203-70-4">132203-70-4</a></span></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> <span style="font-weight:normal"><abbr title="Compound ID">CID</abbr></span></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="pubchem.ncbi.nlm.nih.gov"><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/5282138">5282138</a></span></li></ul></div></td></tr><tr><th scope="row" class="infobox-label" style="line-height:1.2em;"><a href="/wiki/Guide_to_Pharmacology" title="Guide to Pharmacology">IUPHAR/BPS</a></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="www.guidetopharmacology.org"><a rel="nofollow" class="external text" href="https://www.guidetopharmacology.org/GRAC/LigandDisplayForward?ligandId=7767">7767</a></span></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><span title="www.chemspider.com"><a rel="nofollow" class="external text" href="https://www.chemspider.com/Chemical-Structure.4445338.html">4445338</a></span></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><span title="precision.fda.gov"><a rel="nofollow" class="external text" href="https://precision.fda.gov/uniisearch/srs/unii/97T5AZ1JIP">97T5AZ1JIP</a></span></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><span title="www.kegg.jp"><a rel="nofollow" class="external text" href="https://www.kegg.jp/entry/D01173">D01173</a></span></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> <span style="font-weight:normal">(<abbr title="U.S. Environmental Protection Agency">EPA</abbr>)</span></th><td class="infobox-data"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li><span title="comptox.epa.gov"><a rel="nofollow" class="external text" href="https://comptox.epa.gov/dashboard/chemical/details/DTXSID0046309">DTXSID0046309</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q731525#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></span></span></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"><span title="echa.europa.eu">ECHA InfoCard</span></a></th><td class="infobox-data"><a rel="nofollow" class="external text" href="https://echa.europa.eu/substance-information/-/substanceinfo/100.162.338">100.162.338</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q731525#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></span></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"><span title="Carbon">C</span><sub>27</sub><span title="Hydrogen">H</span><sub>28</sub><span title="Nitrogen">N</span><sub>2</sub><span title="Oxygen">O</span><sub>7</sub></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"><span class="nowrap"><span data-sort-value="7002492528000000000♠"></span>492.528</span> g·mol<sup>−1</sup></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><span title="chemapps.stolaf.edu (3D interactive model)"><a rel="nofollow" class="external text" href="https://chemapps.stolaf.edu/jmol/jmol.php?model=O%3DC%28OCCOC%29%5CC2%3DC%28%5CN%2FC%28%3DC%28%2FC%28%3DO%29OC%5CC%3DC%5Cc1ccccc1%29C2c3cccc%28%5BN%2B%5D%28%5BO-%5D%29%3DO%29c3%29C%29C">Interactive image</a></span></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%;">O=C(OCCOC)\C2=C(\N/C(=C(/C(=O)OC\C=C\c1ccccc1)C2c3cccc([N+]([O-])=O)c3)C)C</div></li></ul> </div></td></tr></tbody></table> <p><b>Cilnidipine</b> is a <a href="/wiki/Calcium_channel_blocker" title="Calcium channel blocker">calcium channel blocker</a>. Cilnidipine is approved for use in Japan, China, India, Nepal, and Korea for <a href="/wiki/Hypertension" title="Hypertension">hypertension</a>. </p><p>It is a calcium antagonist accompanied with <a href="/wiki/L-type_calcium_channel" title="L-type calcium channel"><small>L</small>-type</a> and <a href="/wiki/N-type_calcium_channel" title="N-type calcium channel"><small>N</small>-type calcium channel</a> blocking functions. Unlike other calcium antagonists, cilnidipine can act on the <small>N</small>-type calcium channel in addition to acting on the <small>L</small>-type calcium channel. </p><p>It was patented in 1984 and approved for medical use in 1995. Cilnidipine is currently being repurposed and developed for use in patients with Raynaud's Phenomenon and Systemic Sclerosis by Aisa Pharma, a US biopharma development company.<sup id="cite_ref-1" class="reference"><a href="#cite_note-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup> </p> <meta property="mw:PageProp/toc" /> <div class="mw-heading mw-heading2"><h2 id="Medical_uses">Medical uses</h2></div> <p>Cilnidipine decreases blood pressure and is used to treat hypertension and its <a href="/wiki/Comorbidity" title="Comorbidity">comorbidities</a>. Due to its blocking action at the <small>N</small>-type and <small>L</small>-type calcium channel, cilnidipine dilates both <a href="/wiki/Arteriole" title="Arteriole">arterioles</a> and <a href="/wiki/Venule" title="Venule">venules</a>, reducing the pressure in the <a href="/wiki/Capillary_bed" class="mw-redirect" title="Capillary bed">capillary bed</a>. Cilnidipine is vasoselective and has a weak direct <a href="/wiki/Dromotropic" title="Dromotropic">dromotropic</a> effect, a strong vasodepressor effect, and an arrhythmia-inhibiting effect. Blood pressure control with cilnidipine treatment in Japanese post-stroke hypertensive patients [The CA-ATTEND study] - the results of a large-scale prospective post-marketing surveillance study of post-stroke hypertensive patients (n = 2667, male 60.4%, 69.0 ± 10.9 years) treated with cilnidipine indicate that cilnidipine was effective in treating uncontrolled blood pressure and was well tolerated in post-stroke hypertensive patients.<sup id="cite_ref-2" class="reference"><a href="#cite_note-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> The Ambulatory Blood Pressure Control and Home Blood Pressure (Morning and Evening) Lowering By N-Channel Blocker Cilnidipine (ACHIEVE-ONE) trial is a large-scale (n=2319) clinical study on blood pressure (BP) and pulse rate (PR) in the real world with use of cilnidipine - this study revealed that Cilnidipine significantly reduced BP and PR in hypertensive patients at the clinic and at home, especially with higher BP and PR in the morning. Cilnidipine is currently being studied in the RECONNOITER study in Australia for its effect on Raynaud's and other manifestations of disease in patients with Systemic Sclerosis. <sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-4" class="reference"><a href="#cite_note-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="Side_effects">Side effects</h2></div> <p>The side effects could be severe dizziness, fast heartbeat, and swelling of face, lips, tongue, eyelids, hands and feet. Lesser side effects include stomach pain, diarrhea and hypotension. </p><p><a href="/wiki/Peripheral_edema" title="Peripheral edema">Peripheral edema</a>, a common side effect from the use of <a href="/wiki/Amlodipine" title="Amlodipine">amlodipine</a>, was reduced when patients were shifted to cilnidipine.<sup id="cite_ref-5" class="reference"><a href="#cite_note-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="Brand_Name">Brand Name</h2></div> <p>In India, it is sold under the brand name Cinod, cilacar, clinblue, among others at doses of 5mg/10mg/20mg.<sup id="cite_ref-6" class="reference"><a href="#cite_note-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="History">History</h2></div> <p>It was jointly developed by <a href="/w/index.php?title=Fuji_Viscera_Pharmaceutical_Company&action=edit&redlink=1" class="new" title="Fuji Viscera Pharmaceutical Company (page does not exist)">Fuji Viscera Pharmaceutical Company</a> and <a href="/wiki/Ajinomoto" title="Ajinomoto">Ajinomoto</a>, and was approved to enter the market and be used as an <a href="/wiki/Anti-hypertensive" class="mw-redirect" title="Anti-hypertensive">anti-hypertensive</a> in 1995.<sup class="noprint Inline-Template Template-Fact" style="white-space:nowrap;">[<i><a href="/wiki/Wikipedia:Citation_needed" title="Wikipedia:Citation needed"><span title="This claim needs references to reliable sources. (August 2017)">citation needed</span></a></i>]</sup> </p> <div class="mw-heading mw-heading2"><h2 id="References">References</h2></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"><ol class="references"> <li id="cite_note-1"><span class="mw-cite-backlink"><b><a href="#cite_ref-1">^</a></b></span> <span class="reference-text"><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="CITEREFFischerGanellin2006" class="citation book cs1">Fischer J, Ganellin CR (2006). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=FjKfqkaKkAAC&pg=PA466"><i>Analogue-based Drug Discovery</i></a>. John Wiley & Sons. p. 466. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/9783527607495" title="Special:BookSources/9783527607495"><bdi>9783527607495</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Analogue-based+Drug+Discovery&rft.pages=466&rft.pub=John+Wiley+%26+Sons&rft.date=2006&rft.isbn=9783527607495&rft.aulast=Fischer&rft.aufirst=J&rft.au=Ganellin%2C+CR&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DFjKfqkaKkAAC%26pg%3DPA466&rfr_id=info%3Asid%2Fen.wikipedia.org%3ACilnidipine" class="Z3988"></span></span> </li> <li id="cite_note-2"><span class="mw-cite-backlink"><b><a href="#cite_ref-2">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFAokiHosomiNezuTeshima2017" class="citation journal cs1">Aoki S, Hosomi N, Nezu T, Teshima T, Sugii H, Nagahama S, et al. (2017). <a rel="nofollow" class="external text" href="https://doi.org/10.1080%2F10641963.2016.1235183">"Blood pressure control with cilnidipine treatment in Japanese post-stroke hypertensive patients: The CA-ATTEND study"</a>. <i>Clinical and Experimental Hypertension</i>. <b>39</b> (3): 225–234. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://doi.org/10.1080%2F10641963.2016.1235183">10.1080/10641963.2016.1235183</a></span>. <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/28448181">28448181</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Clinical+and+Experimental+Hypertension&rft.atitle=Blood+pressure+control+with+cilnidipine+treatment+in+Japanese+post-stroke+hypertensive+patients%3A+The+CA-ATTEND+study&rft.volume=39&rft.issue=3&rft.pages=225-234&rft.date=2017&rft_id=info%3Adoi%2F10.1080%2F10641963.2016.1235183&rft_id=info%3Apmid%2F28448181&rft.aulast=Aoki&rft.aufirst=S&rft.au=Hosomi%2C+N&rft.au=Nezu%2C+T&rft.au=Teshima%2C+T&rft.au=Sugii%2C+H&rft.au=Nagahama%2C+S&rft.au=Kurose%2C+Y&rft.au=Maruyama%2C+H&rft.au=Matsumoto%2C+M&rft_id=https%3A%2F%2Fdoi.org%2F10.1080%252F10641963.2016.1235183&rfr_id=info%3Asid%2Fen.wikipedia.org%3ACilnidipine" class="Z3988"></span></span> </li> <li id="cite_note-3"><span class="mw-cite-backlink"><b><a href="#cite_ref-3">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFKarioAndoKidoNariyama2013" class="citation journal cs1">Kario K, Ando S, Kido H, Nariyama J, Takiuchi S, Yagi T, et al. 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Registration"</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=ANZCTR+-+Registration&rft_id=https%3A%2F%2Fwww.anzctr.org.au%2FTrial%2FRegistration%2FTrialReview.aspx%3Fid%3D380810%26isReview%3Dtrue&rfr_id=info%3Asid%2Fen.wikipedia.org%3ACilnidipine" class="Z3988"></span></span> </li> <li id="cite_note-5"><span class="mw-cite-backlink"><b><a href="#cite_ref-5">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMinamiKawanoMakinoMatsuoka2000" class="citation journal cs1">Minami J, Kawano Y, Makino Y, Matsuoka H, Takishita S (December 2000). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2015014">"Effects of cilnidipine, a novel dihydropyridine calcium antagonist, on autonomic function, ambulatory blood pressure and heart rate in patients with essential hypertension"</a>. <i>British Journal of Clinical Pharmacology</i>. <b>50</b> (6): 615–20. <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.1365-2125.2000.00299.x">10.1046/j.1365-2125.2000.00299.x</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a> <span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2015014">2015014</a></span>. <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/11136301">11136301</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+Clinical+Pharmacology&rft.atitle=Effects+of+cilnidipine%2C+a+novel+dihydropyridine+calcium+antagonist%2C+on+autonomic+function%2C+ambulatory+blood+pressure+and+heart+rate+in+patients+with+essential+hypertension&rft.volume=50&rft.issue=6&rft.pages=615-20&rft.date=2000-12&rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC2015014%23id-name%3DPMC&rft_id=info%3Apmid%2F11136301&rft_id=info%3Adoi%2F10.1046%2Fj.1365-2125.2000.00299.x&rft.aulast=Minami&rft.aufirst=J&rft.au=Kawano%2C+Y&rft.au=Makino%2C+Y&rft.au=Matsuoka%2C+H&rft.au=Takishita%2C+S&rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC2015014&rfr_id=info%3Asid%2Fen.wikipedia.org%3ACilnidipine" class="Z3988"></span></span> </li> <li id="cite_note-6"><span class="mw-cite-backlink"><b><a href="#cite_ref-6">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="https://medicaldialogues.in/partner/jbcpl/cilacar-cilnidipine">"Cilacar (Cilnidipine): Uses, Side Effects, Dosage - Medical Dialogues"</a>. <a href="/w/index.php?title=Medical_Dialogues&action=edit&redlink=1" class="new" title="Medical Dialogues (page does not exist)">Medical Dialogues</a>. 3 March 2021<span class="reference-accessdate">. Retrieved <span class="nowrap">3 March</span> 2021</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=Cilacar+%28Cilnidipine%29%3A+Uses%2C+Side+Effects%2C+Dosage+-+Medical+Dialogues&rft.pub=Medical+Dialogues&rft.date=2021-03-03&rft_id=https%3A%2F%2Fmedicaldialogues.in%2Fpartner%2Fjbcpl%2Fcilacar-cilnidipine&rfr_id=info%3Asid%2Fen.wikipedia.org%3ACilnidipine" class="Z3988"></span></span> </li> </ol></div></div> <div class="mw-heading mw-heading2"><h2 id="Further_reading">Further reading</h2></div> <style data-mw-deduplicate="TemplateStyles:r1239549316">.mw-parser-output .refbegin{margin-bottom:0.5em}.mw-parser-output .refbegin-hanging-indents>ul{margin-left:0}.mw-parser-output .refbegin-hanging-indents>ul>li{margin-left:0;padding-left:3.2em;text-indent:-3.2em}.mw-parser-output .refbegin-hanging-indents ul,.mw-parser-output .refbegin-hanging-indents ul li{list-style:none}@media(max-width:720px){.mw-parser-output .refbegin-hanging-indents>ul>li{padding-left:1.6em;text-indent:-1.6em}}.mw-parser-output .refbegin-columns{margin-top:0.3em}.mw-parser-output .refbegin-columns ul{margin-top:0}.mw-parser-output .refbegin-columns li{page-break-inside:avoid;break-inside:avoid-column}@media screen{.mw-parser-output .refbegin{font-size:90%}}</style><div class="refbegin" style=""> <ul><li><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFLöhnMuzzuliniEssinTsang2002" class="citation journal cs1">Löhn M, Muzzulini U, Essin K, Tsang SY, Kirsch T, Litteral J, et al. (May 2002). "Cilnidipine is a novel slow-acting blocker of vascular L-type calcium channels that does not target protein kinase C". <i>Journal of Hypertension</i>. <b>20</b> (5): 885–93. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1097%2F00004872-200205000-00023">10.1097/00004872-200205000-00023</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/12011649">12011649</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:30765257">30765257</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+Hypertension&rft.atitle=Cilnidipine+is+a+novel+slow-acting+blocker+of+vascular+L-type+calcium+channels+that+does+not+target+protein+kinase+C&rft.volume=20&rft.issue=5&rft.pages=885-93&rft.date=2002-05&rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A30765257%23id-name%3DS2CID&rft_id=info%3Apmid%2F12011649&rft_id=info%3Adoi%2F10.1097%2F00004872-200205000-00023&rft.aulast=L%C3%B6hn&rft.aufirst=M&rft.au=Muzzulini%2C+U&rft.au=Essin%2C+K&rft.au=Tsang%2C+SY&rft.au=Kirsch%2C+T&rft.au=Litteral%2C+J&rft.au=Waldron%2C+P&rft.au=Conrad%2C+H&rft.au=Klugbauer%2C+N&rft.au=Hofmann%2C+F&rft.au=Haller%2C+H&rft.au=Luft%2C+FC&rft.au=Huang%2C+Y&rft.au=Gollasch%2C+M&rfr_id=info%3Asid%2Fen.wikipedia.org%3ACilnidipine" class="Z3988"></span></li></ul> </div></div><!--esi <esi:include src="/esitest-fa8a495983347898/content" /> --><noscript><img src="https://login.wikimedia.org/wiki/Special:CentralAutoLogin/start?type=1x1&useformat=desktop" alt="" width="1" height="1" style="border: none; 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