Weight | 312.453 g/mol |
---|---|
Formula | C21H28O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
ethisterone (434-03-7)
Pregneninolone · Anhydrohydroxyprogesterone · 17 alpha Ethynyltestosterone
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- THE EFFECTS OF PREGNENINOLONE AND RELATED STEROIDS ON SEXUAL DEVELOPMENT IN FISH (Lebistes reticulatus) (Endocrinology, 1941)
- Randomised trial of high doses of stilboestrol and ethisterone therapy in pregnancy: long-term follow-up of the children. (Journal of Epidemiology and Community Health, 1981)
- Novel C,N-chelate platinum(II) antitumor complexes bearing a lipophilic ethisterone pendant. (Journal of Inorganic Biochemistry, 2011)
- Randomised trial of high doses of stilboestrol and ethisterone in pregnancy: long-term follow-up of mothers. (BMJ, 1980)
- Synthesis and solid state characterization of molecular rotors with steroidal stators: ethisterone and norethisterone (Organic and Biomolecular Chemistry, 2010)
- Click chemistry inspired highly facile synthesis of triazolyl ethisterone glycoconjugates. (Steroids, 2014)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Pregneninolone
- Anhydrohydroxyprogesterone
- 17 alpha Ethynyltestosterone
- 17 alpha-Ethynyltestosterone
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SMILESCC12CCC(=O)C=C1CCC3C2CCC4(C3CCC4(C#C)O)C
-
InChIKeyCHNXZKVNWQUJIB-UHFFFAOYSA-N
- Pubchem - ethisterone
- Wikipedia - ethisterone
Ethisterone (brand names Proluton C, Pranone among others), also known as ethinyltestosterone, pregneninolone, or anhydrohydroxyprogesterone, is a progestin with androgenic activity which was derived from testosterone and was introduced for medical use in 1939. It was the second progestogen to be marketed (intramuscular progesterone was introduced as Proluton in 1934) and was both the first orally active progestogen and the first progestin (synthetic progestogen) to be introduced. Although ethisterone has largely been superseded by newer drugs and is now little used, it reportedly continues to be available in some countries.
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