| Weight | 268.356 g/mol |
|---|---|
| Formula | C18H20O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
equilin (474-86-2)
Score:
#1381 in Biochemistry
,
#3323 in Biology
,
#4145 in Chemistry
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- Structure of the ternary complex of human 17-hydroxysteroid dehydrogenase type 1 with 3-hydroxyestra-1,3,5,7-tetraen-17-one (equilin) and NADP+ (Proceedings of the National Academy of Sciences of the United States of America, 1999)
- Equilin, a Principal Component of the Estrogen Replacement Therapy Premarin, Increases the Growth of Cortical Neurons via an NMDA Receptor-Dependent Mechanism (Experimental Neurology, 1997)
- The major metabolite of equilin, 4-hydroxyequilin, autoxidizes to an o-quinone which isomerizes to the potent cytotoxin 4-hydroxyequilenin-o-quinone. (Chemical Research in Toxicology, 1999)
- Serum equilin and conjugated equine oestrogens. (The Lancet, 1976)
- Oestrone and equilin in the plasma of the pregnant mare. (Journal of reproduction and fertility, 1975)
- SERUM EQUILIN, STRONE, AND STRADIOL LEVELS IN POSTMENOPAUSAL WOMEN RECEIVING CONJUGATED EQUINE STROGENS ('PREMARIN') (The Lancet, 1980)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC12CCC3C(=CCC4=C3C=CC(=C4)O)C1CCC2=O
-
InChIKeyWKRLQDKEXYKHJB-UHFFFAOYSA-N
- Pubchem - equilin
- Wikipedia - equilin
Equilin, also known as 7-dehydroestrone, as well as estra-1,3,5(10),7-tetraen-3-ol-17-one, is an estrogen from horses. Equilin is one of the estrogens present in the mixture of estrogens isolated from horse urine and marketed as Premarin. Premarin became the most commonly used form of estrogen for hormone replacement therapy in the United States of America.
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