| Weight | 296.41 g/mol |
|---|---|
| Formula | C20H24O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
ethinyl estradiol (57-63-6)
Estinyl · Ethinyloestradiol · Ethynyl Estradiol
Score:
#3 in Biochemistry
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#37 in Biology
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#38 in Chemistry
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- Ethinyloestradiol an undesired fish contraceptive? (Aquatic Toxicology, 1999)
- Ethinyl estradiol acutely attenuates abnormal coronary vasomotor responses to acetylcholine in postmenopausal women. (Circulation, 1994)
- Increased binding of low density lipoprotein to liver membranes from rats treated with 17 alpha-ethinyl estradiol. (Journal of Biological Chemistry, 1979)
- Degradation of endocrine disrupting chemicals bisphenol A, Ethinyl estradiol, and estradiol during UV photolysis and advanced oxidation processes (Environmental Science & Technology, 2004)
- Adsorption and Hysteresis of Bisphenol A and 17-Ethinyl Estradiol on Carbon Nanomaterials (Environmental Science & Technology, 2008)
- Endocrine and metabolic effects of metformin versus ethinyl estradiol-cyproterone acetate in obese women with polycystic ovary syndrome: a randomized study. (The Journal of Clinical Endocrinology and Metabolism, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Estinyl
- Ethinyloestradiol
- Ethynyl Estradiol
- Lynoral
- Ethinyl Estradiol, (8 alpha,9 beta,13 alpha,14 beta)-Isomer
- Ethinyl Estradiol, (8 alpha)-Isomer
- Ethinyl Estradiol, (8 alpha,17 alpha)-Isomer
- Schering Brand of Ethinyl Estradiol
- Ethinyl Estradiol Hemihydrate
- Ethinyl Estradiol, (9 beta,17 alpha)-Isomer
- Progynon C
- Effik Brand of Ethinyl Estradiol
- Microfollin
- Jenapharm Brand of Ethinyl Estradiol
- Schering-Plough Brand of Ethinyl Estradiol
- Ethinyl-Oestradiol Effik
- Organon Brand of Ethinyl Estradiol
- Ethinyl Oestradiol Effik
- Ethinylestradiol Jenapharm
- Microfollin Forte
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SMILESCC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)O
-
InChIKeyBFPYWIDHMRZLRN-UHFFFAOYSA-N
- Pubchem - ethinyl estradiol
- Wikipedia - Ethinylestriol
Ethinylestriol (EE3), or 17-ethynylestriol, also known as 17-ethynylestra-1,3,5(10)-triene-3,16,17-triol, is a synthetic, steroidal estrogen that was never marketed. Nilestriol, the 3-cyclopentyl ether of ethinylestriol, is a prodrug of ethinylestriol, and is a more potent estrogen in comparison, but, similarly to ethinylestriol, was never marketed. Ethinylestriol has been found to reduce the risk of 7,12-dimethylbenz(a)anthracene (DMBA)-induced mammary cancer when given as a prophylactic in animal models, while other estrogens like ethinylestradiol and diethylstilbestrol were ineffective.
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ethinyl estradiol
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