Synthesis and structure-activity relationships of 2-vinylchroman-4-ones as potent antibiotic agents

被引:92
作者
Albrecht, U
Lalk, M
Langer, P
机构
[1] Univ Greifswald, Inst Pharm, D-17487 Greifswald, Germany
[2] Univ Greifswald, Int Chem & Biochem, D-17487 Greifswald, Germany
关键词
antibiotics; chromanones; natural product analogues; oxygen heterocycles; pharmacological screening;
D O I
10.1016/j.bmc.2004.12.031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of novel 2-vinylchroman-4-ones, analogues of the natural products Aposphaerin A and B, were identified as potent antibiotics. Derivatives exhibit a significant activity against multiresistant strains of S. aureus, such as MRSA (methicillin resistant S. aureus). The 2-vinylchroman-4-ones were efficiently prepared by Lewis acid mediated conjugate addition of vinylmagnesium bromide to chromones. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1531 / 1536
页数:6
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