专利检索 ap:("LATVIAN INSTITUTE OF ORGANIC SYNTHESIS") AND inv:"SAINT-LEGER, Adelaide" 第 1 页

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发明申请
NOVEL N-ACYL-ARYLSULFONAMIDE DERIVATIVES AS AMINOACYL-TRNA SYNTHETASE INHIBITORS 审中-公开
标题翻译：新型N-亚氨基磺酰胺衍生物作为氨基酰基-TNA合成酶抑制剂

公开(公告)号：WO2016129983A1

公开(公告)日：2016-08-18

申请号：PCT/LV2016/000001

申请日：2016-02-11

申请人： LATVIAN INSTITUTE OF ORGANIC SYNTHESIS

发明人： JIRGENSONS, Aigars , LOZA, Einars , CHARLTON, Michael , FINN, Paul William , RIBAS DE POUPLANA, Lluis , SAINT-LEGER, Adelaide

IPC分类号： C07D213/71 , C07D311/20 , C07D215/36 , C07D217/22 , C07C311/00 , C07D239/42 , C07D239/47 , C07D239/48 , C07D251/22 , C07D487/04 , A61K31/4402 , A61K31/47 , A61K31/505 , A61K31/18 , A61P31/00

CPC分类号： C07C311/51 , C07C2601/02 , C07D213/71 , C07D215/06 , C07D215/36 , C07D217/04 , C07D217/22 , C07D217/26 , C07D239/42 , C07D239/47 , C07D239/48 , C07D251/22 , C07D311/04 , C07D311/20 , C07D487/04

摘要： The present invention relates to novel N-acyl-diarysulfonamides acting as inhibitors of bacterial aminoacyl-tRNA synthetase. These can be used as medicines or as constituent of medicines for the treatment of bacterial infections.

摘要翻译： 本发明涉及作为细菌氨酰-tRNA合成酶抑制剂的新型N-酰基 - 二芳基磺酰胺。这些可用作药物或用作治疗细菌感染的药物的组成部分。