Enzymatic conversion of 32-oxygenated Δ7-lanosterol derivatives and of Δ8(14)-4,4-dimethyl-cholestenol to cholesterol
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference10 articles.
1. THE BIOSYNTHESIS OF CHOLESTEROL FROM ACETATE-1-C14 BY CELLULAR FRACTIONS OF RAT LIVER
2. Pathways of Enzymic Synthesis and Conversion to Cholesterol of Δ5,7,24-Cholestatrien-3β-ol and Other Naturally Occurring Sterols
3. Sterol Biosynthesis
4. 32-Hydroxylated lanostane derivatives by photolysis of 3β-acetoxy-7-ketolanostane
5. Rearrangements of 32-oxygenated lanostanes
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1. The mode of incorporation of C-2 hydrogen atoms of mevalonic acid into protosterols and sterols;Tetrahedron;1986-01
2. The Biosynthesis of Ergosterol;Pesticide Science;1984-04
3. Sterol Biosynthesis;Annual Review of Biochemistry;1982-06
4. Sterol synthesis. A simplified method for the synthesis of 32-oxygenated derivatives of 24,25-dihydrolanosterol.;Journal of Lipid Research;1981-07
5. Utilization and metabolism of methyl-sterol derivatives in the yeast mutant strain GL7;Biochemistry;1981-05-01
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