17α-Dihydroequilenin
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| ファイル:17α-Dihydroequilenin.svg | |
|---|---|
| Systematic (IUPAC) name | |
| (13S,14S,17R)-13-methyl-11,12,14,15,16,17-hexahydrocyclopenta[a]phenanthrene-3,17-diol | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Routes | By mouth |
| Identifiers | |
| CAS number | 6639-99-2 
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| ATC code | ? |
| PubChem | CID 223998 |
| ChemSpider | 194598 |
| UNII | D9ZR4ZMP2S
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| ChEBI | CHEBI:34178 |
| ChEMBL | CHEMBL135236 |
| Synonyms | NSC-12171; α-Dihydroequilenin; 6,8-Didehydro-17α-estradiol; Estra-1,3,5(10),6,8-pentaen-3,17α-diol |
| Chemical data | |
| Formula | C18H20O2 |
| SMILES | eMolecules & PubChem |
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17α-Dihydroequilenin, or α-dihydroequilenin, also known as 6,8-didehydro-17α-estradiol, as well as estra-1,3,5(10),6,8-pentaen-3,17α-diol, is a naturally occurring steroidal estrogen found in horses which is closely related to equilin, equilenin, and 17α-estradiol, and, as the 3-sulfate ester sodium salt, is a minor constituent (1.2%) of conjugated estrogens (Premarin).[1]
See also
References
- ↑ Fritz MA, Speroff L (28 March 2012). Clinical Gynecologic Endocrinology and Infertility. Lippincott Williams & Wilkins. pp. 751–. ISBN 978-1-4511-4847-3.
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