Utilization of precursor steroids in placental progesterone**The trivial names used throughout this paper are: progesterone=preg-4-ene-3, 20-dione; pregnenolone=3β-hydroxy-pregn-5-en-20-one; cholesterol=cholest-5-en-3β-ol; 20α-dihydroprogesterone=20α-hydroxy-pregn-4-en-3-one; 20β-dihydroprogesterone=20β-hydroxy-pregn-4-en-3-one; 20β-dihydropregnenolone=pregn-5-ene-3β, 20β-diol; 20α-dihydropregnenolone=pregn-5-ene-3β, 20a-diol; pregnenolone sulfate=pregn-5-ene-3β-yl sulfate; cholesterol sulfate=cholest-5-en-3β-yl sulfate; 20β-pregnenolone sulfate=20β-hydroxypregn-5-en-3β-yl sulfate; 20α-dihydroprogesterone sulfate=pregn-4-ene-3-one-20α-yl sulfate. synthesis
Autor: | Ronald J. Pion, Suzanne H. Conrad, James D. Kitchin, Pei-Chuan Ouyang |
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Rok vydání: | 1969 |
Předmět: | |
Zdroj: | American Journal of Obstetrics and Gynecology. 103:48-55 |
ISSN: | 0002-9378 |
DOI: | 10.1016/s0002-9378(16)34339-3 |
Popis: | A number of radioactive steroid and sterol compounds were infused into the human term placenta in situ in an effort to assess their potential as precursors for progesterone production. Pregnenolone and pregnenolone sulfate were most efficiently converted to progesterone (12.8 and 12.9 per cent of injected radioactive material). 20β-dihydroprogesterone, 20β-dihydropregnenolone, and 20β-dihydropregnenolone-3-sulfate were converted in very low yield ( |
Databáze: | OpenAIRE |
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