| Weight | 328.452 g/mol |
|---|---|
| Formula | C21H28O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Nomegestrol (58691-88-6)
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- Cardiovascular risk factors and combined estrogen-progestin replacement therapy: a placebo-controlled study with nomegestrol acetate and estradiol (Fertility and Sterility, 1995)
- Effects of a monophasic combined oral contraceptive containing nomegestrol acetate and 17-oestradiol compared with one containing levonorgestrel and ethinylestradiol on haemostasis, lipids and carbohydrate metabolism (The European Journal of Contraception & Reproductive Health Care, 2011)
- Reversal effects of nomegestrol acetate on multidrug resistance in adriamycin-resistant MCF7 breast cancer cell line (Breast Cancer Research, 2001)
- Effects of nomegestrol acetate (5 mg/d) on hormonal, metabolic and hemostatic parameters in premenopausal women (Contraception, 1991)
- Efficacy and tolerability of a monophasic combined oral contraceptive containing nomegestrol acetate and 17-oestradiol in a 24/4 regimen, in comparison to an oral contraceptive containing ethinylestradiol and drospirenone in a 21/7 regimen (The European Journal of Contraception & Reproductive Health Care, 2011)
- Effect of nomegestrol acetate, a new 19-nor-progesterone derivative, on pituitary-ovarian function in women (British Journal of Obstetrics and Gynaecology, 1987)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC2C(CCC3(C2CCC3(C(=O)C)O)C)C4C1=CC(=O)CC4
-
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- Pubchem - Nomegestrol
- Wikipedia - nomegestrol
Nomegestrol (INN), also known as 19-normegestrol, is a steroidal progestin which was patented in 1975 but was never marketed. It is the parent compound of nomegestrol acetate, which is marketed as a progestin.
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