| Weight | 266.34 g/mol |
|---|---|
| Formula | C18H18O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
EQUILENIN (517-09-9)
Score:
#73 in Molecular and cellular biology
,
#2154 in Biochemistry
,
#5576 in Chemistry
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- The Total Synthesis of the Sex Hormone Equilenin and Its Stereoisomers (Journal of the American Chemical Society, 1940)
- A new synthesis of fused ring structure related to the steroids; the 17-equilenones; a total synthesis of equilenin. (Journal of the American Chemical Society, 1947)
- Crystal structure of Delta(5)-3-ketosteroid isomerase from Pseudomonas testosteroni in complex with equilenin settles the correct hydrogen bonding scheme for transition state stabilization (Journal of Biological Chemistry, 1999)
- Novel total syntheses of (+)-estrone 3-methyl ether, (+)-13.beta.-ethyl-3-methoxygona-1,3,5(10)-trien-17-one, and (+)-equilenin 3-methyl ether (Journal of Organic Chemistry, 1975)
- THE TOTAL SYNTHESIS OF THE SEX HORMONE EQUILENIN (Journal of the American Chemical Society, 1939)
- Excited-state proton transfer of equilenin and dihydroequilenin: interaction with bilayer vesicles. (Biochemistry, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC12CCC3=C(C1CCC2=O)C=CC4=C3C=CC(=C4)O
-
InChIKeyPDRGHUMCVRDZLQ-UHFFFAOYSA-N
- Pubchem - EQUILENIN
- Wikipedia - equilenin
Equilenin, also known as 6,8-didehydroestrone, as well as estra-1,3,5(10),6,8-pentaen-3-ol-17-one, is an estrogenic steroid hormone obtained from the urine of pregnant mares. It is used as one of the components in Premarin. It was the first complex natural product to be fully synthesized, in work reported by 1940 by Bachmann and Wilds.
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EQUILENIN
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