Literature DB >> 6577424

Natural 25,26-dihydroxyvitamin D3 is an epimeric mixture.

N Ikekawa, N Koizumi, E Ohshima, S Ishizuka, T Takeshita, Y Tanaka, H F DeLuca.   

Abstract

Radiolabeled 25,26-dihydroxyvitamin D3 was prepared in vitro by using chicken kidney homogenates and in vivo in rats from [23,24-3H]-25-hydroxyvitamin D3. These compounds were mixed with synthetic (25S)- and (25R)-25,26-dihydroxyvitamin D3, converted to the corresponding (+)-alpha-methoxy-alpha-trifluoromethylphenylacetyl esters, and subjected to high-performance liquid chromatography that separates the derivatized epimers. The radiolabeled 25,26-dihydroxyvitamin D3 derivatives were a 1:1 mixture of the 25S and 25R isomers. Similarly unlabeled 25,26-dihydroxyvitamin D3 isolated from the plasma of rats given large amounts of vitamin D3 was shown to be a 1:1 mixture of the S and R isomers. Therefore, naturally occurring 25,26-dihydroxyvitamin D3 is a mixture of the 25R and 25S isomers and not just the S isomer reported previously.

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Year:  1983        PMID: 6577424      PMCID: PMC384238          DOI: 10.1073/pnas.80.17.5286

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  13 in total

1.  Letter: Stereospecificity in the conversion of fucosterol 24,28-epoxide to desmosterol in the silkworm, Bombyx mori.

Authors:  S M Chen; K Nakanishi; N Awata; M Morisaki; N Ikekawa
Journal:  J Am Chem Soc       Date:  1975-09-03       Impact factor: 15.419

2.  Determination of stereochemical configuration of the 24-hydroxyl group of 24,25-dihydroxyvitamin D3 and its biological importance.

Authors:  Y Tanaka; H F DeLuca; N Ikekawa; M Morisaki; N Koizumi
Journal:  Arch Biochem Biophys       Date:  1975-10       Impact factor: 4.013

3.  Carbon-13 NMR studies on cholesterol biosynthesized from [13C]mevalonates.

Authors:  G Popják; J Edmond; F A Anet; N R Easton
Journal:  J Am Chem Soc       Date:  1977-02-02       Impact factor: 15.419

4.  The absolute configuration of the natural 25,26-dihydroxycholecalciferol.

Authors:  J Redel; N Bazely; Y Tanaka; H F DeLuca
Journal:  FEBS Lett       Date:  1978-10-15       Impact factor: 4.124

5.  The configuration at C-25 of human 25,26-dihydroxycholecalciferol.

Authors:  J Redel; N Bazely; E B Mawer; J Hann; F S Jones
Journal:  FEBS Lett       Date:  1979-10-01       Impact factor: 4.124

6.  Measurement of mammalian 25-hydroxyvitamin D3 24R-and 1 alpha-hydroxylase.

Authors:  Y Tanaka; H F DeLuca
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

7.  The 24-hydroxylation of 1,25-dihydroxyvitamin D3.

Authors:  Y Tanaka; L Castillo; H F DeLuca
Journal:  J Biol Chem       Date:  1977-02-25       Impact factor: 5.157

8.  Stereochemical importance of fucosterol epoxide in the conversion of sitosterol into cholesterol in the silkworm Bombyx mori.

Authors:  Y Fujimoto; M Morisaki; N Ikekawa
Journal:  Biochemistry       Date:  1980-03-18       Impact factor: 3.162

9.  On the stereospecificity of cholestanetriol 26-monooxygenase.

Authors:  Y Atsuta; K Okuda
Journal:  J Biol Chem       Date:  1981-09-10       Impact factor: 5.157

10.  On the stereospecificity of microsomal "26"-hydroxylation in bile acid biosynthesis.

Authors:  J Gustafsson; S Sjöstedt
Journal:  J Biol Chem       Date:  1978-01-10       Impact factor: 5.157

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  2 in total

Review 1.  The serum vitamin D metabolome: What we know and what is still to discover.

Authors:  Robert C Tuckey; Chloe Y S Cheng; Andrzej T Slominski
Journal:  J Steroid Biochem Mol Biol       Date:  2018-09-08       Impact factor: 4.292

Review 2.  Reminiscences of research on the chemistry and biology of natural sterols in insects, plants and humans.

Authors:  Nobuo Ikekawa; Yoshinori Fujimoto; Masaji Ishiguro
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2013       Impact factor: 3.493

  2 in total

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