Microbial hydroxylation of ML-236B (compactin) Studies on microorganisms capable of 3.BETA.-hydroxylation of ML-236B.

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Taxonomy of actinomycetes capable of hydroxylation of ML-236B (compactin).

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Formation of dihydroxy derivative of ML-236B from ML-236B (compactin) by lipid peroxidation.

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Growth inhibition of yeast by compactin (ML-236B) analogues.

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The synthesis of compactin (ML-236B) and monacolin K in fungi.

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ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogenesis produced by Penicillium citrinium.

Sir: Clinical and nutritional studies have indicated that high cholesterol levels in the blood may be one of the major causes of atherosclerosis and coronary heart disease. In this context the metabolism of cholesterol in liver is of paramount importance because liver seems to be the sole organ supplying serum cholesterol and because the conversion of cholesterol into bile acids in liver is qua...

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ژورنال

عنوان ژورنال: The Journal of Antibiotics

سال: 1983

ISSN: 0021-8820,1881-1469

DOI: 10.7164/antibiotics.36.887