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

作者信息

Yamashita H, Tsubokawa S, Endo A

出版信息

J Antibiot (Tokyo). 1985 May;38(5):605-9. doi: 10.7164/antibiotics.38.605.

DOI:10.7164/antibiotics.38.605
PMID:4040510
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.

摘要

相似文献

1
Microbial hydroxylation of compactin (ML-236B) and monacolin K.
J Antibiot (Tokyo). 1985 May;38(5):605-9. doi: 10.7164/antibiotics.38.605.
2
Microbial phosphorylation of compactin (ML-236B) and related compounds.
J Antibiot (Tokyo). 1985 Mar;38(3):328-32. doi: 10.7164/antibiotics.38.328.
3
Microbial hydroxylation of ML-236B (compactin) and monacolin K (MB-530B).ML-236B(美伐他汀)和莫纳可林K(MB-530B)的微生物羟基化作用
J Antibiot (Tokyo). 1983 May;36(5):604-7. doi: 10.7164/antibiotics.36.604.
4
3 alpha-Hydroxy-ML-236B (3 alpha-hydroxycompactin), microbial transformation product of ML-236B (compactin).
J Antibiot (Tokyo). 1983 May;36(5):608-10. doi: 10.7164/antibiotics.36.608.
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Monacolin M, a new inhibitor of cholesterol biosynthesis.莫纳可林M,一种新的胆固醇生物合成抑制剂。
J Antibiot (Tokyo). 1986 Dec;39(12):1670-3. doi: 10.7164/antibiotics.39.1670.
6
Purification and characterization of cytochrome P-450sca from Streptomyces carbophilus. ML-236B (compactin) induces a cytochrome P-450sca in Streptomyces carbophilus that hydroxylates ML-236B to pravastatin sodium (CS-514), a tissue-selective inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme-A reductase.嗜碳链霉菌中细胞色素P-450sca的纯化与特性分析。ML-236B(美伐他汀)可诱导嗜碳链霉菌产生一种细胞色素P-450sca,该细胞色素可将ML-236B羟化为普伐他汀钠(CS-514),一种3-羟基-3-甲基戊二酰辅酶A还原酶的组织选择性抑制剂。
Eur J Biochem. 1989 Oct 1;184(3):707-13. doi: 10.1111/j.1432-1033.1989.tb15070.x.
7
Formation of dihydroxy derivative of ML-236B from ML-236B (compactin) by lipid peroxidation.
J Antibiot (Tokyo). 1990 Aug;43(8):1031-3. doi: 10.7164/antibiotics.43.1031.
8
Biochemical aspect of HMG CoA reductase inhibitors.
Adv Enzyme Regul. 1989;28:53-64. doi: 10.1016/0065-2571(89)90063-0.
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Biosynthesis of ML-236B (compactin) and monacolin K.ML-236B(美伐他汀)和莫纳可林K的生物合成
J Antibiot (Tokyo). 1985 Mar;38(3):444-8. doi: 10.7164/antibiotics.38.444.
10
Biosynthesis of monacolins: conversion of monacolin J to monacolin K (mevinolin).
J Antibiot (Tokyo). 1990 Dec;43(12):1621-2. doi: 10.7164/antibiotics.43.1621.

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