Enzymatic isomerization (Δ7 → Δ8) of the nuclear double bond of 14α-alkyl substituted sterol precursord of cholesterol
- 1 June 1980
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 94 (3) , 932-939
- https://doi.org/10.1016/0006-291x(80)91324-8
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Enzymatic conversion of 5α‐cholesta‐7,14‐dien‐3β‐ol to 5α‐cholesta‐8,14‐dien‐3β‐olLipids, 1975
- The Reversibility of the Isomerization of the Δ8 to Δ7 Bond in Cholesterol BiosynthesisEuropean Journal of Biochemistry, 1974
- Studies of the Metabolism of 5α-Cholesta-8,14-dien-3β-ol and 5α-Cholesta-7,14-dien-3β-ol in Rat Liver Homogenate PreparationsPublished by Elsevier ,1971
- Studies on the Mechanism of the Enzymatic Conversion of Δ8-Cholesten-3β-ol to Δ7-Cholesten-3β-olJournal of Biological Chemistry, 1969
- The stereochemistry of hydrogen elimination in the biological conversion of 5α-cholest-8-en-3β-ol to 5α-cholest-7-en-3β-olSteroids, 1968
- Stereospecificity in the Enzymatic Conversion of Δ7-Cholesten-3β-ol to 7-DehydrocholesterolPublished by Elsevier ,1968
- Sterol BiosynthesisAnnual Review of Biochemistry, 1967
- Enzymatic isomerization (Δ8 → Δ7) of intermediates of sterol biosynthesisSteroids, 1966
- The Biological Synthesis of CholesterolScience, 1965
- Biosynthesis of sterols, steroids, and terpenoids. Part I. Biogenesis of cholesterol and the fundamental steps in terpenoid biosynthesisQuarterly Reviews, Chemical Society, 1965