Metabolism of [17-2H]pregnenolone into 5-[17β-2H, 17α-[18O]androstene-3β,17α-diol and other products by incubation with the microsomal fraction of boar testis under 18O2 atmosphere
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry,Biophysics
Reference12 articles.
1. Formation of 5-[17beta-2H]androstene-3beta,17alpha-diol from 3beta-hydroxy-5-[17,21,21,21-2H]pregnen-20-one by the microsomal fraction of boar testis.
2. Synthesis and study of the labeling of pregnenolone and progesterone specifically tritiated at the 17 position.
3. Formation of [17-2H]androsta-5,16-dien-3β-ol from [17,21,21,21]pregnenolone by the microsomal fraction of boar testis
4. PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
5. Gas chromatographic and mass spectrometric studies of oximes derived from 20-oxosteroids
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2. The diverse chemistry of cytochrome P450 17A1 (P450c17, CYP17A1);The Journal of Steroid Biochemistry and Molecular Biology;2015-07
3. Use of gas chromatographic-mass spectrometric techniques in studies of androst-16-ene and androgen biosynthesis in human testis; cytosolic specific binding of 5α-androst-16-en-3-one;The Journal of Steroid Biochemistry and Molecular Biology;1997-01
4. Mechanism of the Acyl-Carbon Cleavage and Related Reactions Catalyzed by Multifunctional P-450s: Studies on Cytochrome P-45017.alpha.;Biochemistry;1994-04-12
5. 16-ene-steroids in the human testis;The Journal of Steroid Biochemistry and Molecular Biology;1991-01
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