Estradiol 17β-acetate
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ファイル:Estradiol acetate.svg | |
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Systematic (IUPAC) name | |
[(8R,9S,13S,14S,17S)-3-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] acetate | |
Clinical data | |
Pregnancy cat. | ? |
Legal status | ? |
Identifiers | |
CAS number | 1743-60-8 |
ATC code | ? |
PubChem | CID 6852404 |
ChemSpider | 5254726 |
UNII | 2VM9HO33RU |
KEGG | C15228 |
ChEBI | CHEBI:79735 |
ChEMBL | CHEMBL1611800 |
Chemical data | |
Formula | C20H26O3 |
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Estradiol 17β-acetate is an estrogen and an estrogen ester—specifically, the C17β acetate ester of estradiol—which was never marketed.[1][2][3] It is the C17β positional isomer of the better-known and clinically used estradiol ester estradiol acetate (estradiol 3-acetate; Femtrace).[1]
See also
References
- ↑ 以下の位置に戻る: 1.0 1.1 Junkmann K, Witzel H (1957). "Chemie und Pharmakologie von Steroidhormon-Estern" [Chemistry and pharmacology of steroid hormone esters]. Z Vitam Horm Fermentforsch (in Deutsch). 9 (1–2): 97–143 contd. PMID 13531579.
- ↑ Janocko L, Larner JM, Hochberg RB (April 1984). "The interaction of C-17 esters of estradiol with the estrogen receptor". Endocrinology. 114 (4): 1180–6. doi:10.1210/endo-114-4-1180. PMID 6705734.
- ↑ Mu Y, Peng S, Zhang A, Wang L (February 2011). "Role of pocket flexibility in the modulation of estrogen receptor alpha by key residue arginine 394". Environ. Toxicol. Chem. 30 (2): 330–6. Bibcode:2011EnvTC..30..330M. doi:10.1002/etc.389. PMID 21038436. S2CID 22116062.
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- Abandoned drugs
- Acetate esters
- Estradiol esters
- Secondary alcohols
- Synthetic estrogens