Clinical data | |
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Other names | NSC-12171; α-Dihydroequilenin; 6,8-Didehydro-17α-estradiol; Estra-1,3,5(10),6,8-pentaen-3,17α-diol |
Routes of administration | By mouth |
Drug class | Estrogen |
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ChEMBL | |
ECHA InfoCard | 100.026.955 |
Chemical and physical data | |
Formula | C18H20O2 |
Molar mass | 268.356 g·mol−1 |
3D model (JSmol) | |
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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.
ERTooltip Estrogen receptor |
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GPERTooltip G protein-coupled estrogen receptor |
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