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从黄萎轮枝菌中分离得到的新型呋咱吡酮类化合物作为有效的抗真菌物质。

Novel neofusapyrones isolated from Verticillium dahliae as potent antifungal substances.

机构信息

Faculty of Agriculture and Life Science, Hirosaki University, 3 Bunkyo-Cho, Hirosaki, Aomori 036-8561, Japan.

出版信息

Bioorg Med Chem Lett. 2010 Jan 15;20(2):709-12. doi: 10.1016/j.bmcl.2009.11.063. Epub 2009 Dec 3.

DOI:10.1016/j.bmcl.2009.11.063
PMID:19962895
Abstract

Novel fusapyrone analogs, deoxyneofusapyrone and 7-desmethyldeoxyneofusapyrone were isolated from a pathogenic fungus, Verticillium dahliae, which causes Verticillium wilt disease in Helianthus annuus. Spectral analyses revealed that these are 2-pyrone type analogs of deoxyfusapyrone and its 7-desmethyl derivative, respectively. Biological assay disclosed that 10microg of deoxyneofusapyrone inhibited the growth of MRSA clinical isolate 87-7927.

摘要

新型 Fusapyrone 类似物,脱氧 Neofusapyrone 和 7-去甲脱氧 Neofusapyrone 从致病真菌 Verticillium dahliae 中分离出来,该真菌可引起向日葵的黄萎病。光谱分析表明,它们分别是脱氧 Fusapyrone 和其 7-去甲基衍生物的 2-吡喃酮类类似物。生物测定表明,脱氧 Neofusapyrone 的 10μg 抑制了 MRSA 临床分离株 87-7927 的生长。

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