Synthetic studies on V-ATPase inhibiting macrolide antibiotics

被引：8

作者：

Toshima, K ^{[1
]}

机构：

[1] Keio Univ, Fac Sci & Technol, Dept Appl Chem, Yokohama, Kanagawa 2238522, Japan

来源：

CURRENT ORGANIC CHEMISTRY | 2004年 / 8卷 / 02期

关键词：

D O I：

10.2174/1385272043486043

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Synthetic studies on the specific inhibitors of vacuolar-type H+-ATPase, bafilomycins, hygrolidines, and concanamycins, are described. Bafilomycins and hygrolidins are 16-membered and concanamycins are 18-membered plecomacrolides, which have very complex molecular structures.

引用

页码：185 / 210

页数：26

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