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L-8.2888 -60.3322 L-7.2888 -60.3322 L-7.2888 -56.6916 L-2.7732 -56.6916 L-2.7732 -60.3322 L-1.7732 -60.3322 L-1.7732 -51.7697 Z"></path><path style="fill:black; stroke:none;" d="M26.1358 -51.6587 L25.1358 -51.6587 L25.1358 -55.69 L20.6202 -55.69 L20.6202 -51.6587 L19.6202 -51.6587 L19.6202 -60.2212 L20.6202 -60.2212 L20.6202 -56.5806 L25.1358 -56.5806 L25.1358 -60.2212 L26.1358 -60.2212 L26.1358 -51.6587 Z"></path><path style="fill:black; stroke:none;" d="M46.3648 34.0933 L45.3648 34.0933 L45.3648 30.062 L40.8492 30.062 L40.8492 34.0933 L39.8492 34.0933 L39.8492 25.5308 L40.8492 25.5308 L40.8492 29.1714 L45.3648 29.1714 L45.3648 25.5308 L46.3648 25.5308 L46.3648 34.0933 Z"></path></g></g></svg></svg></svg></svg></div></app-svg-box></div></app-multi-image><h3 _ngcontent-sc115="" class="name">CAS Name</h3><span _ngcontent-sc115="" class="casName">Galeterone</span><h3 _ngcontent-sc115="" class="molecularFormula">Molecular Formula</h3><span _ngcontent-sc115="" id="molform">C<sub>26</sub>H<sub>32</sub>N<sub>2</sub>O</span><h3 _ngcontent-sc115="" class="molecularMass">Molecular Mass</h3> 388.55 <button _ngcontent-sc115="" class="view-sfn-button">Discover more in SciFinder</button><div _ngcontent-sc115="" class="page-citation"><h3 _ngcontent-sc115="">Cite this Page</h3><span _ngcontent-sc115="" class="name">Galeterone</span>.   <em _ngcontent-sc115="">CAS Common Chemistry</em>.   CAS, a division of the American Chemical Society, n.d.   <span _ngcontent-sc115="" class="url">http://commonchemistry.cas.org/detail?cas_rn=851983-85-2</span> (retrieved <span _ngcontent-sc115="" class="timestamp">2025-03-18</span>) (CAS RN: <span _ngcontent-sc115="" class="casRn">851983-85-2</span>).  Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). </div></div></detail-summary></div><div _ngcontent-sc118="" class="col-lg-8 col-md-7 no-padding"><detail-ancillary _ngcontent-sc118="" _nghost-sc117=""><div _ngcontent-sc117="" class="detail-content-box detail-content-box-right"><h2 _ngcontent-sc117="" class="compoundPropertiesHeader">Compound Properties</h2><ul _ngcontent-sc117="" class="properties"><li _ngcontent-sc117=""><h3 _ngcontent-sc117="" class="property-name">Melting Point (1)</h3><span _ngcontent-sc117="" class="property-value">189-190 °C</span></li></ul><h3 _ngcontent-sc117="">Source(s)</h3><ul _ngcontent-sc117="" class="sources"><li _ngcontent-sc117=""><span _ngcontent-sc117=""><a _ngcontent-sc117="" href="#goToSfn">(1) Handratta, Venkatesh D.; Journal of Medicinal Chemistry, (2005), 48(8), 2972-2984, CAplus</a></span></li></ul></div></detail-ancillary><detail-info _ngcontent-sc118="" _nghost-sc116=""><div _ngcontent-sc116="" class="detail-content-box detail-content-box-right"><h2 _ngcontent-sc116="">Other Names and Identifiers</h2><h3 _ngcontent-sc116="" class="inchi">InChI</h3><p _ngcontent-sc116="" class="identifier">InChI=1S/C26H32N2O/c1-25-13-11-18(29)15-17(25)7-8-19-20-9-10-24(26(20,2)14-12-21(19)25)28-16-27-22-5-3-4-6-23(22)28/h3-7,10,16,18-21,29H,8-9,11-15H2,1-2H3/t18-,19-,20-,21-,25-,26-/m0/s1</p><h3 _ngcontent-sc116="" class="inchiKey">InChIKey</h3><p _ngcontent-sc116="" class="identifier">InChIKey=PAFKTGFSEFKSQG-PAASFTFBSA-N</p><h3 _ngcontent-sc116="" class="smile">SMILES</h3><p _ngcontent-sc116="" class="identifier">C[C@@]12[C@]([C@]3([C@](CC1)([C@]4(C)C(=CC3)C[C@@H](O)CC4)[H])[H])(CC=C2N5C=6C(N=C5)=CC=CC6)[H]</p><h3 _ngcontent-sc116="" class="canonicalSmile">Canonical SMILES</h3><p _ngcontent-sc116="" class="identifier">OC1CC2=CCC3C4CC=C(N5C=NC=6C=CC=CC65)C4(C)CCC3C2(C)CC1</p><h3 _ngcontent-sc116="" class="synonyms">Other Names for this Substance</h3><div _ngcontent-sc116="" class="detail-synonym-box"><ul _ngcontent-sc116=""><li _ngcontent-sc116="">Androsta-5,16-dien-3-ol, 17-(1<em>H</em>-benzimidazol-1-yl)-, (3β)-</li><li _ngcontent-sc116="">(3β)-17-(1<em>H</em>-Benzimidazol-1-yl)androsta-5,16-dien-3-ol</li><li _ngcontent-sc116="">VN/124-1</li><li _ngcontent-sc116="">VN 124</li><li _ngcontent-sc116="">Galeterone</li></ul></div><div _ngcontent-sc116="" class="synonyms-toggle"><p _ngcontent-sc116=""><a _ngcontent-sc116="">View All</a></p></div><p _ngcontent-sc116=""></p></div></detail-info></div></div><div _ngcontent-sc118="" class="insight-teaser"><app-insight-teaser _ngcontent-sc118="" _nghost-sc107=""><div _ngcontent-sc107="" class="row teaser-header cas-blue">CAS INSIGHTS<sup _ngcontent-sc107="">TM</sup></div><div _ngcontent-sc107="" class="teaser-container"><div _ngcontent-sc107="" class="teaser text-black"><div _ngcontent-sc107="" class="teaser-img"><a _ngcontent-sc107="" target="_blank" class="insight-teaser-link" href="https://www.cas.org/resources/topic/drug-discovery?utm_campaign=GLO_GEN_ANY_CIS_AWS&utm_medium=SYN_CAS_ORG&utm_source=CommonChemistry"><img _ngcontent-sc107="" 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By using CAS Common Chemistry, you agree to the terms and conditions of this license. </div></app-license></div></div><ngx-json-ld _ngcontent-sc118=""><script type="application/ld+json">{ "@context": "http://schema.org", "@type": "ChemicalSubstance", "name": "Galeterone", "url": "http://commonchemistry.cas.org/detail?cas_rn=851983-85-2", "hasBioChemEntityPart": { "@type": "MolecularEntity", "name": "Galeterone", "identifier": "InChI=1S/C26H32N2O/c1-25-13-11-18(29)15-17(25)7-8-19-20-9-10-24(26(20,2)14-12-21(19)25)28-16-27-22-5-3-4-6-23(22)28/h3-7,10,16,18-21,29H,8-9,11-15H2,1-2H3/t18-,19-,20-,21-,25-,26-/m0/s1", "molecularFormula": "C<sub>26</sub>H<sub>32</sub>N<sub>2</sub>O" }, "chemicalComposition": "C<sub>26</sub>H<sub>32</sub>N<sub>2</sub>O", "alternateNames": [ "Androsta-5,16-dien-3-ol, 17-(1<em>H</em>-benzimidazol-1-yl)-, (3β)-", "(3β)-17-(1<em>H</em>-Benzimidazol-1-yl)androsta-5,16-dien-3-ol", "VN/124-1", "VN 124", "Galeterone", "TOK 001", "Galaterone", "TK-001" ] 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