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
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