「3β-Hydroxytibolone」の版間の差分
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bsd>حسن علي البط (added Category:Tertiary alcohols using HotCat) |
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2025年3月18日 (火) 19:27時点における最新版
| ファイル:3β-Hydroxytibolone.svg | |
|---|---|
| Systematic (IUPAC) name | |
| (3S,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 | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 100239-45-0 |
| ATC code | ? |
| PubChem | CID 9839851 |
| ChemSpider | 8015569 |
| UNII | TEP8IU9GMR |
| Synonyms | ORG-30126; 7α-Methyl-17α-ethynylestr-5(10)-ene-3β,17β-diol |
| Chemical data | |
| Formula | C21H30O2 |
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3β-Hydroxytibolone (developmental code name ORG-30126) is a synthetic steroidal estrogen which was never marketed.[1][2] Along with 3α-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.[1][2]
References
- ↑ 1.0 1.1 Kuhl, H (2005). "Pharmacology of estrogens and progestogens: influence of different routes of administration". Climacteric. 8 (sup1): 3–63. doi:10.1080/13697130500148875. ISSN 1369-7137. PMID 16112947. S2CID 24616324.
- ↑ 2.0 2.1 Escande A, Servant N, Rabenoelina F, Auzou G, Kloosterboer H, Cavaillès V, Balaguer P, Maudelonde T (2009). "Regulation of activities of steroid hormone receptors by tibolone and its primary metabolites". J. Steroid Biochem. Mol. Biol. 116 (1–2): 8–14. doi:10.1016/j.jsbmb.2009.03.008. PMID 19464167. S2CID 18346113.
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