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filingDate 1981-06-08^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-07-19^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44de608adb5d9c2df5307bacc008fc48
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publicationDate 1983-07-19^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1150170-A
titleOfInvention Ml-236b derivatives and their preparation
abstract Abstract the disclosure Compounds of formula (I): (I) (wherein R represents d group of formula or and the corresponding ring-closed lactones, salts (especially alkali metal salts) and esters (especially C1-C5 alkyl esters) thereof may be prepared by subjecting ML-236B, or ML-236B carboxylic acid or a salt or ester thereof to enzymatic hydroxylation, which may be effected by means of microorganisms of the genera Mucor, Rhizopus, Zygorynchus, Circinella, Actinomucor, Gongronella, Phycomyces, Martierella, Pycnoporus, Rhizoctonia, Absidia, Cunninghamella, Syncephalosporum and Streptomyces, or cell-free, enzyme-containing extracts from said microorganisms. The compounds are capable of inhibiting biosynthesis of cholesterol and are thus useful in the treatment of hypercholesteraemia.
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priorityDate 1980-06-06^^<http://www.w3.org/2001/XMLSchema#date>
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