Suppr超能文献

F - 244特异性抑制3 - 羟基 - 3 - 甲基戊二酰辅酶A合酶。

F-244 specifically inhibits 3-hydroxy-3-methylglutaryl coenzyme A synthase.

作者信息

Tomoda H, Kumagai H, Tanaka H, Omura S

机构信息

Kitasato Institute, Tokyo, Japan.

出版信息

Biochim Biophys Acta. 1987 Dec 14;922(3):351-6.

PMID:2891379
Abstract

A beta-lactone isolated from Scopulariopsis sp. shows a potent inhibition of cholesterogenesis. The structure of this beta-lactone, termed F-244, is 3,5,7-trimethyl-12-hydroxy-13-hydroxymethyl-2,4-tetradecadiendioic acid 12,14-lactone. The inhibition site of F-244 in cholesterol synthesis was studied. The growth of Vero cells was inhibited at 6.25-12.5 micrograms/ml of F-244. The inhibition of growth was overcome by the addition of mevalonate to the culture medium, but not by the addition of acetate. In a rat liver enzyme system, the incorporations of [14C]acetate and [14C]acetyl-CoA into digitonin-precipitable sterol were 50% inhibited by 0.58 microgram/ml of F-244. The incorporation of [14C]mevalonate was not affected. Studies on the effects of F-244 on the three enzymes involved in mevalonate biosynthesis demonstrated that the drug specifically inhibits HMG-CoA synthase with IC50 value of 0.065 microgram/ml. The effect of analogs of F-244 on HMG-CoA synthase was also investigated.

摘要

从帚霉属真菌中分离出的一种β-内酯对胆固醇合成有强烈抑制作用。这种被称为F-244的β-内酯的结构为3,5,7-三甲基-12-羟基-13-羟甲基-2,4-十四碳二烯二酸12,14-内酯。研究了F-244在胆固醇合成中的抑制位点。当F-244浓度为6.25 - 12.5微克/毫升时,Vero细胞的生长受到抑制。向培养基中添加甲羟戊酸可克服生长抑制,但添加乙酸则不能。在大鼠肝脏酶系统中,0.58微克/毫升的F-244可使[14C]乙酸和[14C]乙酰辅酶A掺入洋地黄皂苷可沉淀固醇的量被抑制50%。[14C]甲羟戊酸的掺入不受影响。对F-244对甲羟戊酸生物合成中涉及的三种酶的作用的研究表明,该药物特异性抑制HMG-CoA合酶,IC50值为0.065微克/毫升。还研究了F-244类似物对HMG-CoA合酶的作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验