| Weight | 308.421 g/mol |
|---|---|
| Formula | C21H24O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Gestrinone (16320-04-0)
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- Sigma-Aldrich - Search for Gestrinone
- Fisher Scientific - Search for Gestrinone
- TCI - Gestrinone208.00 USD
- Impact of gestrinone on the course of asymptomatic endometriosis (BMJ, 1987)
- Gestrinone versus danazol in the treatment of endometriosis (Fertility and Sterility, 1989)
- The inhibitory effects of danazol, danazol metabolites, gestrinone, and testosterone on the growth of human endometrial cells in vitro (Fertility and Sterility, 1988)
- Long-term treatment of leiomyomas with gestrinone * (Fertility and Sterility, 1989)
- Treatment of endometriosis with gestrinone (R-2323), a synthetic antiestrogen, antiprogesterone (American Journal of Obstetrics and Gynecology, 1982)
- Discovery, Biosynthesis, and Structure Elucidation of Metabolites of a Doping Agent and a Direct Analogue, Tetrahydrogestrinone and Gestrinone, Using Human Hepatocytes (Analytical Chemistry, 2005)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCC12C=CC3=C4CCC(=O)C=C4CCC3C1CCC2(C#C)O
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InChIKeyBJJXHLWLUDYTGC-UHFFFAOYSA-N
- Pubchem - Gestrinone
- Wikipedia - gestrinone
Gestrinone, sold under the brand names Dimetriose, Dimetrose, and Nemestran among others, is a synthetic steroid that is used in the treatment of endometriosis. It has mixed progestogenic and antiprogestogenic, weak androgenic, antigonadotropic, and functional antiestrogen activity. Gestrinone is described as similar in action and effect to danazol, which is also used in the treatment of endometriosis, but is reported to have fewer androgenic side effects in comparison.
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Gestrinone
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