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Inhibitors of UDP-galactopyranose mutase

机译:UDP-吡喃半乳糖突变酶的抑制剂

摘要

Compounds and salts thereof which inhibit microbial growth or attenuate the virulence of pathogenic microorganisms and which inhibit UDP-galactopyranose mutase (UGM). Compounds of the invention include triazolothiadiazines, particularly 3,6,7-substituted-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines, and 4-(1H-pyrrol-3-yl) thiazoles, particularly 4-(1,2,5-substituted-1H-pyrrol-3-yl)-2-substituted thiazoles, and salts thereof. Methods for inhibiting growth or attenuating virulence of microbial pathogens including mycobacterium, for example, M. tuberculosis and M. smegmatis and Klebsiella, for example, Klebsiella pneumoniae. Methods for inhibiting eukaryotic human and animal pathogens, and fungi and nematodes in particular. Methods for treatment of infections by prokaryotic and eukaryotic pathogens employing compounds of the invention.
机译:抑制微生物生长或减弱病原微生物毒力并抑制UDP-吡喃半乳糖突变酶(UGM)的化合物及其盐。本发明的化合物包括三唑并噻二嗪,特别是3,6,7-取代的7H- [1,2,4]三唑并[3,4-b] [1,3,4]噻二嗪和4-(1H-吡咯- 3-基)噻唑,特别是4-(1,2,5-取代的-1H-吡咯-3-基)-2-取代的噻唑及其盐。抑制微生物病原体包括分枝杆菌例如I.M的生长或减弱其毒力的方法。结核 M。包皮垢克雷伯菌,例如肺炎克雷伯菌。抑制真核人和动物病原体,特别是抑制真菌和线虫的方法。使用本发明的化合物治疗原核和真核病原体感染的方法。

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