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Inhibitors of p38-alpha kinase

机译:p38-α激酶抑制剂

摘要

The invention is directed to methods to treat conditions mediated by p38-alphakinase using compounds of the formulaand the pharmaceutically acceptable salts thereof, or a pharmaceutical composition thereof,whereinZ is N or CR1, R1 is a noninterfering substituent,each of X1 and X2 is a linker,Ar1 and Ar2 are identical or different, and represent optionally substituted C1-C20 hydrocarbyl residues wherein at least one of Ar1 and Ar2 is an optionally substituted aryl group, with the proviso that when X2 is CH2 or an isostere thereof, X1 is CO or an isostere thereof, and Ar2 is optionally substituted phenyl, Ar1 is other than an optionally substituted indolyl, benzimidazolyl or benzotriazolyl substituent, and wherein said optionally substituted phenyl is not an optionally substituted indolyl, benzimidazolyl, or benzotriazolyl,Y is a noninterfering substituent, wherein n is an integer from 0-4, andwherein m is an integer from 0-4 and 1 is an integer from 0-3.
机译:本发明涉及使用下式的化合物及其药学上可接受的盐或其药物组合物治疗由p38-α激酶介导的病症的方法,其中Z为N或CR1,R1为非干扰取代基,X1和X2均为A。接头,Ar 1和Ar 2相同或不同,并且表示任选取代的C 1 -C 20烃基残基,其中Ar 1和Ar 2至少一个是任选取代的芳基,条件是当X 2为CH 2或其等排体时,X 1为CO。或其等排体,并且Ar 2是任选取代的苯基,Ar 1不是任选取代的吲哚基,苯并咪唑基或苯并三唑基取代基,并且其中所述任选取代的苯基不是任选取代的吲哚基,苯并咪唑基或苯并三唑基,Y是非干扰取代基,其中,n是0-4的整数,其中m是0-4的整数,1是0-3的整数。

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