Weight | 298.426 g/mol |
---|---|
Formula | C20H26O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
norethindrone (68-22-4)
Norethisterone · Micronor · Norlutin
Score:
#40 in Biochemistry
,
#218 in Biology
,
#228 in Chemistry
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- Circulating Nitric Oxide (Nitrite/Nitrate) Levels in Postmenopausal Women Substituted With 17-Estradiol and Norethisterone Acetate A Two-Year Follow-up Study (Hypertension, 1995)
- 17-Estradiol and Continuous Norethisterone: A Unique Treatment for Established Osteoporosis in Elderly Women (The Journal of Clinical Endocrinology and Metabolism, 1990)
- Randomised comparative trial of the levonorgestrel intrauterine system and norethisterone for treatment of idiopathic menorrhagia. (British Journal of Obstetrics and Gynaecology, 1998)
- The effects of norethisterone in postmenopausal women on oestrogen replacement therapy: a model for the premenstrual syndrome (British Journal of Obstetrics and Gynaecology, 1986)
- Treatment of endometriosis and chronic pelvic pain with letrozole and norethindrone acetate: a pilot study (Fertility and Sterility, 2004)
- Effect of Topiramate on the Pharmacokinetics of an Oral Contraceptive Containing Norethindrone and Ethinyl Estradiol in Patients with Epilepsy (Epilepsia, 1997)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Norethisterone
- Micronor
- Norlutin
- Norcolut
- Norpregneninolone
- Monogest
- Norcolute
- NorQD
- Conceplan
- Nor-QD
- Norethindrone, (1 beta)-Isomer
- Nor QD
- Ethinylnortestosterone
-
SMILESCC12CCC3C(C1CCC2(C#C)O)CCC4=CC(=O)CCC34
-
InChIKeyVIKNJXKGJWUCNN-UHFFFAOYSA-N
- Pubchem - norethindrone
- Wikipedia - norethindrone
Norethisterone (NET), also known as norethindrone, is a medication that is used in combination with estrogen or alone in hormonal contraceptives, menopausal hormone therapy, and in the treatment of gynecological disorders. It is a synthetic progestogen (or a progestin) of the 19-nortestosterone group and has similar effects to those of natural progesterone, including suppression of gonadotropins, ovulation inhibition, and endometrial transformation. In addition to its progestogenic activity, NET also has weak androgenic and estrogenic effects at high dosages.
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