Literature DB >> 4040510

Microbial hydroxylation of compactin (ML-236B) and monacolin K.

H Yamashita, S Tsubokawa, A Endo.   

Abstract

The Basidiomycete Schizophyllum commune was found to transform compactin (ML-236B) to 8a-hydroxycompactin. This compound was isolated by solvent extraction and column chromatography, and its structure was determined by a combination of IR, UV, 1H NMR and 13C NMR spectroscopy. Monacolin K was also converted to the corresponding hydroxylated analogue. Data on the inhibition of 3-hydroxy-3-methylglutaryl co-enzyme A reductase and sterol biosynthesis in vitro are presented for these hydroxylated compounds.

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Year:  1985        PMID: 4040510     DOI: 10.7164/antibiotics.38.605

Source DB:  PubMed          Journal:  J Antibiot (Tokyo)        ISSN: 0021-8820            Impact factor:   2.649


  2 in total

1.  Microbial conversion products of leptomycin B.

Authors:  M Kuhnt; F Bitsch; M Ponelle; J J Sanglier; Y Wang; B Wolff
Journal:  Appl Environ Microbiol       Date:  1998-02       Impact factor: 4.792

Review 2.  Chemistry, biochemistry, and pharmacology of HMG-CoA reductase inhibitors.

Authors:  A Endo
Journal:  Klin Wochenschr       Date:  1988-05-16
  2 in total

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