FLUVIRUCIN-A1, FLUVIRUCIN-A2, FLUVIRUCIN-B1, FLUVIRUCIN-B2, FLUVIRUCIN-B3, FLUVIRUCIN-B4, AND FLUVIRUCIN-B5, NEW ANTIBIOTICS ACTIVE AGAINST INFLUENZA-A VIRUS .1. PRODUCTION, ISOLATION, CHEMICAL-PROPERTIES AND BIOLOGICAL-ACTIVITIES

被引:50
作者
NARUSE, N
TENMYO, O
KAWANO, K
TOMITA, K
OHGUSA, N
MIYAKI, T
KONISHI, M
OKI, T
机构
[1] Bristol-Myers Squibb Research Institute, Meguro-ku, Tokyo 153
关键词
D O I
10.7164/antibiotics.44.733
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Five unidentified actinomycete strains produced a series of novel antiviral antibiotics which have a unique 2,6-dialkyl-10-ethyl-3(or 9)-hydroxy-13-tridecanelactam nucleus substituted with 3-amino-3,6-dideoxy-L-talose or 3-amino-3,6-dideoxy-L-mannose(L-mycosamine). The antibiotic components exhibited potent inhibitory activity against influenza virus type A Victoria strain infection in Madin Darby canine kidney cells by the cytopathic effect reduction assay.
引用
收藏
页码:733 / 740
页数:8
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