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Synthesis of 25-hydroxy-(26,27-/sup 3/H)vitamin D2, 1,25-dihydroxy-(26,27-/sup 3/H)vitamin D2 and their (24R)-epimers

Journal Article · · Anal. Biochem.; (United States)
; ; ; ;
Synthesis of a C-24-epimeric mixture of 25-hydroxy-(26,27-/sup 3/H)vitamin D2 and a C-24-epimeric mixture of 1,25-dihydroxy-(26,27-/sup 3/H)vitamin D2 by the Grignard reaction of the corresponding 25-keto-27-nor-vitamin D2 and 1 alpha-acetoxy-25-keto-27-nor-vitamin D3 with tritiated methyl magnesium bromide is described. Separation of epimers by high-performance liquid chromatography afforded pure radiolabeled vitamins of high specific activity (80 Ci/mmol). The identities and radiochemical purities of 25-hydroxy-(26,27-/sup 3/H(vitamin D2 and 1,25-dihydroxy-(26,27-/sup 3/H)vitamin D2 D2 were established by cochromatography with synthetic 25-hydroxyvitamin D2 or 1,25-dihydroxyvitamin D2. Biological activity of 25-hydroxy-(26,27-/sup 3/H)vitamin D2 was demonstrated by its binding to the rat plasma binding protein for vitamin D compounds, and by its in vitro conversion to 1,25-dihydroxy-(26,27-/sup 3/H)vitamin D2 by kidney homogenate prepared from vitamin D-deficient chickens. The biological activity of 1,25-dihydroxy-(26,27-/sup 3/H)vitamin D2 was demonstrated by its binding to the chick intestinal receptor for 1,25-dihydroxyvitamin D3.
Research Organization:
Univ. of Wisconsin, Madison
OSTI ID:
6501041
Journal Information:
Anal. Biochem.; (United States), Journal Name: Anal. Biochem.; (United States) Vol. 1; ISSN ANBCA
Country of Publication:
United States
Language:
English

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Related Subjects

550201* -- Biochemistry-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ANIMALS
BIOCHEMICAL REACTION KINETICS
BIRDS
CHEMICAL PREPARATION
CHICKENS
CHROMATOGRAPHY
CPB
ERGOCALCIFEROL
FOWL
IN VITRO
ISOTOPE APPLICATIONS
KINETICS
LABELLED COMPOUNDS
LIQUID COLUMN CHROMATOGRAPHY
MAMMALS
RATS
REACTION KINETICS
RODENTS
SEPARATION PROCESSES
SYNTHESIS
TRACER TECHNIQUES
TRITIUM COMPOUNDS
VERTEBRATES
VITAMIN D
VITAMINS