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2-AMINO-N-(ARYLSULFINYL)-ACETAMIDE COMPOUNDS AS INHIBITORS OF BACTERIAL AMINOACYL-TRNA SYNTHETASE
专利权人:
Oxford Drug Design Limited
发明人:
Paul William FINN,Michael CHARLTON,Grace EDMUND,Aigars JIRGENSONS,Einars LOZA
申请号:
US16339542
公开号:
US20200039929A1
申请日:
2017.10.06
申请国别(地区):
US
年份:
2020
代理人:
摘要:
The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain 2-amino-N-(arylsulfinyl)-acetamide compounds that, inter alia, inhibit (e.g., selectively inhibit) bacterial aminoacyl-tRNA synthetase (aaRS) (e.g., bacterial leucyl-t RNA synthetase, LeuRS). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit (e.g., selectively inhibit) bacterial aminoacyl-tRNA synthetase; to treat disorders that are ameliorated by the inhibition (e.g., selective inhibition) of bacterial aminoacyl-tRNA synthetase; to treat bacterial infections; etc.
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中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/
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