Enzymatic conversion of cholest-8(14)-en-3β,15α-diol and cholest-8(14)-en-3β,15β-diol to cholesterol

Autor:	S. Huntoon, G.J. Schroepfer
Rok vydání:	1970
Předmět:	chemistry.chemical_classification Cholesterol ALUMINUM HYDRIDE Diol Biophysics chemistry.chemical_element Cell Biology Biochemistry Medicinal chemistry chemistry.chemical_compound Enzyme chemistry Rat liver Organic chemistry Lithium Cholesterol formation Epimer Molecular Biology
Zdroj:	Biochemical and Biophysical Research Communications. 40:476-480
ISSN:	0006-291X
DOI:	10.1016/0006-291x(70)91033-8
Popis:	Reduction of 3β-benzoyloxy-cholest-8(14)-en 13-one with lithium aluminum hydride yielded two epimers (at C-15) of cholest-8(14)-en-3β,15-diol. Reduction with lithium aluminum tritide yielded [15α-3H]-cholest-8(14)-en-3β,15β-diol and [15β-3H]-cholest-8(14)-en-3β,155-diol. Both labeled compounds served as efficient substrates for cholesterol formation in rat liver homogenate preparations.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f074805839bfab73fc8f6644dc3576e7 https://doi.org/10.1016/0006-291x(70)91033-8 Zobrazit plný text záznamu