17β-Dihydroequilin
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| Clinical data | |
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| Routes of administration | Oral |
| Identifiers | |
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| Synonyms | NSC-12170 |
| CAS Number | 3563-27-7 |
| PubChem (CID) | 11954027 |
| ChemSpider | 10128322 |
| UNII | WXG88DST4R |
| ChEBI | CHEBI:62851 |
| ChEMBL | CHEMBL121458 |
| Chemical and physical data | |
| Formula | C18H22O22 |
| Molar mass | 270.36608 g/mol |
| 3D model (Jmol) | Interactive image |
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17β-Dihydroequilin, or β-dihydroequilin, also known as 7-dehydro-17β-estradiol, as well as estra-1,3,5(10),7-tetraen-3,17β-diol, is a naturally occurring steroidal estrogen found in horses that is closely related to equilin, equilenin, and estradiol, and, as the 3-sulfate ester sodium salt, is a minor constituent (1.7%) of conjugated equine estrogens (Premarin).[1]
See also
- 17α-Dihydroequilin
- 17α-Dihydroequilenin
- 17β-Dihydroequilenin
- 8,9-Dehydroestrone
- 8,9-Dehydroestradiol
References
- ↑ Marc A. Fritz; Leon Speroff (28 March 2012). Clinical Gynecologic Endocrinology and Infertility. Lippincott Williams & Wilkins. pp. 751–. ISBN 978-1-4511-4847-3.
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See also: Androgenics • Glucocorticoidics • Mineralocorticoidics • Progestogenics • Steroid hormone metabolism modulators | |||||||||||
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