| Weight | 298.426 g/mol |
|---|---|
| Formula | C20H26O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
norethynodrel (68-23-5)
Norethynodrel, (8 alpha)-(+-)-Isomer
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- Subcellular distribution of 3-H-estradiol in rat uterus by quantitative autoradiography--a comparison between 3-H-estradiol and 3-H-norethynodrel. (Endocrinology, 1968)
- Effects of norethynodrel and progesterone on hepatic microsomal drug-metabolizing enzyme systems (Biochemical Pharmacology, 1966)
- Oral contraception by norethynodrel: A 3 year field study (American Journal of Obstetrics and Gynecology, 1961)
- Histology of the uterus and ovaries after long-term cyclic norethynodrel therapy (American Journal of Obstetrics and Gynecology, 1964)
- Inherent Estrogenicity of Norethindrone and Norethynodrel: Comparison with Other Synthetic Progestins and Progesterone1 (The Journal of Clinical Endocrinology and Metabolism, 1962)
- Metabolic Fate of Orally Administered H3-Norethynodrel in Rabbits (Endocrinology, 1962)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Norethynodrel, (8 alpha)-(+-)-Isomer
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SMILESCC12CCC3C(C1CCC2(C#C)O)CCC4=C3CCC(=O)C4
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InChIKeyICTXHFFSOAJUMG-UHFFFAOYSA-N
- Pubchem - norethynodrel
- Wikipedia - norethynodrel
Noretynodrel, or norethynodrel, is a progestin of the 19-nortestosterone group and an isomer of norethisterone. Noretynodrel was introduced in 1957 in Enovid, a combination formulation of noretynodrel and mestranol, for the treatment of gynecological and menstrual disorders. A few years later, in May 1960, Enovid was also approved as the first oral contraceptive.
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