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Compounds for inhibiting AGC kinase and pharmaceutical compositions comprising the same
专利权人:
Industrial Technology Research Institute
发明人:
Chih-Hung Chen,Yi-Hsun Chen,Jui-Wen Huang,Kuo-Kuei Huang,Chih-Peng Liu,Chrong-Shiong Hwang
申请号:
US16206000
公开号:
US10696638B2
申请日:
2018.11.30
申请国别(地区):
US
年份:
2020
代理人:
摘要:
A compound of formula (I) or a pharmaceutically acceptable salt thereof is provided. In formula (I), Ar is indazole, 5-isoquinoline, 6-isoquinoline, or their N-oxide. X is —;C(═;Z)—;, wherein Z is N—;CN, NH, NR4, NCOR4, NCONR4R5, NCO-aryl, S, or O. Y and J are independently H, alkyl, aryl, aminoalkyl, —;NH2, —;CN, —;OH, —;O-alkyl, —;O-aryl, —;COOH, —;COOR4, —;CONHR4, —;CONHCH2-aryl, —;CONR4CH2-aryl, —;NHCOR4, halogen, halogened alkyl, -alkyl-OR4, -alkyl-ONO2, alkyl-ONO2, —;OCOOR4, —;O(C═;O)-aryl, —;CHR4OH, —;CH2OH, —;CH2O(C═;O)-aryl, —;CH2O(C═;O)—;R4, —;CHR4O(C═;O)-aryl, —;CHR4O(C═;O)—;R4, unsaturated carboxylic ester, substituted alkynyl, —;NHSO2R4, —;SO2R4, —;SO2NHR4, or —;SO2NR4R5, or Y and J bond together to form a carbocylic or aromatic ring, wherein R4 and R5 are independently H, substituted C1-C6 alkyl, substituted aryl, cycloalkyl, alkylaryl, -alkyl-NR6R7, —;S(O)0-2-(alkyl-NR6R7). R1, R2 and R3 are H, C1-C6 alkyl, cycloalkyl, aryl, alkylaryl, alkylheteroaryl, alkylheterocycle, wherein any one thereof is optionally substituted with one or more of OH, NO2, or NR8R9.
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