1955
DOI: 10.1210/endo-57-2-200
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BIOGENESIS OF THE ESTROGENS: THE CONVERSION OF TESTOSTERONE-4-C14TO ESTRONE IN THE PREGNANT MARE1

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Cited by 59 publications
(8 citation statements)
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“…Three recrystallizations yielded specific activities of 131, 149, and 127 respectively. The conversion of Cig steroids to estrogens has been amply demonstrated (5,11,12) and the fact that the Ci 9 -19-hydroxy compound is an intermediate in estrogen biosynthesis strongly indicated (1, 2, 3). It has now been demonstrated for the first time that in an incubation using a human placental preparation with A 4 -androstene-3,17-dione as the substrate that in addition to a good yield of estrone, 19-hydroxy-A 4 -androstene-3,17-dione could be demonstrated.…”
Section: Methodsmentioning
confidence: 99%
“…Three recrystallizations yielded specific activities of 131, 149, and 127 respectively. The conversion of Cig steroids to estrogens has been amply demonstrated (5,11,12) and the fact that the Ci 9 -19-hydroxy compound is an intermediate in estrogen biosynthesis strongly indicated (1, 2, 3). It has now been demonstrated for the first time that in an incubation using a human placental preparation with A 4 -androstene-3,17-dione as the substrate that in addition to a good yield of estrone, 19-hydroxy-A 4 -androstene-3,17-dione could be demonstrated.…”
Section: Methodsmentioning
confidence: 99%
“…These views were later sup ported by the finding that increased excretion of estrogens accompanied the administration of androgens to man (129)(130)(131). Proof for the conversion of androgens to estrogens in the body was obtained by Heard and colleagues (132,133) who isolated radioactive estrone from the urine after administra tion of testosterone-4-C14 to a pregnant mare. Comparison of the yield in this experiment with the formation of radioactive estrogens from acetate made it unlikely that the administered steroid had undergone extensive degradation.…”
Section: Estrogen Biosynthesis and Aromatization Of Steroidsmentioning
confidence: 98%
“…The former was separated into ketonic and non-ketonic fractions by treatment with Girard's reagent T (Girard & Sandulesco, 1936). Oestrone and equilenin were separated by elution with benzene from a column of Celite impregnated with 0-4 N-NaOH solution (Heard, Jellinck & O'Donnell, 1955).…”
Section: Methodsmentioning
confidence: 99%