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3α-Hydroxytibolone
| Column 1 |
|---|
| ORG-4094; 7α-Methyl-17α-ethynylestr-5(10)-ene-3α,17β-diol |
| IUPAC name |
| (3R,7R,8R,9S,13S,14S,17R)-17-Ethynyl-7,13-dimethyl-2,3,4,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol |
| .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}100239-44-9 |
| 10087021 |
| 8262558 |
| 37T303O94A |
| DTXSID001315905 |
| C21H30O2 |
| 314.469 g·mol−1 |
| Interactive image |
| SMILES |
| C[C@@H]1CC2=C(CCC@HO)[C@@H]3[C@@H]1[C@@H]4CCC@(C#C)O |
| InChI |
| InChI=1S/C21H30O2/c1-4-21(23)10-8-18-19-13(2)11-14-12-15(22)5-6-16(14)17(19)7-9-20(18,21)3/h1,13,15,17-19,22-23H,5-12H2,2-3H3/t13-,15-,17-,18+,19-,20+,21+/m1/s1Key:YLEUWNOTNJZCBN-CZTKNSHGSA-N |
3α-Hydroxytibolone (developmental code name ORG-4094) is a synthetic steroidal estrogen which was never marketed. Along with 3β-hydroxytibolone and δ4-tibolone, it is a major active metabolite of tibolone, and 3α-hydroxytibolone and 3β-hydroxytibolone are thought to be responsible for the estrogenic activity of tibolone.
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