Stereochemical specificity at carbon-20 and -22 of hydroxylated cholesterols for side-chain cleavage by adrenocortical cytochrome P -450scc
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(76)80999-4/fullpdf
Reference17 articles.
1. Purification of cytochrome P-450 from bovine adrenocortical mitochondria by an “Aniline-sepharose” and the properties
2. Cholesterol 20,22-epoxides: No conversion to pregnenolone by adrenal cytochrome P-450scc
3. Pregnenolone formation from cholesterol in bovine adrenal cortex mitochondria: Proposal of a new mechanism
4. Evidence for 20, 22-epoxycholesterol as an intermediate in side-chain cleavage of 22R-OH cholesterol by adrenal cortex mitochondria
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2. C-C bond cleavage reactions catalyzed by cytochrome P450 enzymes;Medicinal Chemistry Research;2023-05-27
3. Reflections on sterol sidechain cleavage process catalyzed by cytochrome P450scc;The Journal of Steroid Biochemistry and Molecular Biology;2001-07
4. Regio- and stereo-selective oxidation of steroids using 2,6-dichloropyridine N-oxide catalysed by ruthenium porphyrins;Chemical Communications;1997
5. Purification and comparative characterization of cytochrome P-450scc (CYP XIA1) from sheep adrenocortical mitochondria;Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism;1994-11
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