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拓扑异构酶II:新型抗真菌药物的潜在靶点。

Topoisomerase II: a potential target for novel antifungal agents.

作者信息

Figgitt D P, Denyer S P, Dewick P M, Jackson D E, Williams P

机构信息

Department of Pharmaceutical Sciences, University of Nottingham, University Park, U.K.

出版信息

Biochem Biophys Res Commun. 1989 Apr 14;160(1):257-62. doi: 10.1016/0006-291x(89)91649-5.

Abstract

Several podophyllotoxin-related lignans have been shown to possess significant antifungal activity against a number of filamentous fungi. Initial structure-activity studies indicate this action is sensitive to change at the 4 and 4' positions of the podophyllotoxin skeleton. Good correlation has been observed between antifungal action and the ability to inhibit the relaxation of supercoiled plasmid DNA by a topoisomerase II preparation from Saccharomyces cerevisiae. Etoposide, an inhibitor of mammalian topoisomerase II, is inactive against this yeast enzyme, although good inhibition is shown by amiloride, 4'-(9-acridinylamino)-methanesulphon-m-anisidide (m-AMSA) and novobiocin, known inhibitors of the mammalian enzyme.

摘要

几种鬼臼毒素相关的木脂素已被证明对多种丝状真菌具有显著的抗真菌活性。初步的构效关系研究表明,这种作用对鬼臼毒素骨架4位和4'位的变化敏感。已观察到抗真菌作用与抑制酿酒酵母拓扑异构酶II制剂对超螺旋质粒DNA松弛能力之间具有良好的相关性。依托泊苷是一种哺乳动物拓扑异构酶II的抑制剂,对这种酵母酶无活性,而阿米洛利、4'-(9-吖啶基氨基)-甲磺基间茴香胺(m-AMSA)和新生霉素(已知的哺乳动物酶抑制剂)则表现出良好的抑制作用。

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