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6-ALCOXYPYRIDOPYRIMIDINES AND PHARMACEUTICAL COMPOUND POSSESSING ACTIVITY OF MAP p38 KINASE INHIBITORS

机译:MAP p38激酶抑制剂的6-羟吡啶吡啶酮类和药物复方活性

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to the formula I compounds or its pharmaceutically acceptable salt or hydrate where Z means N; X1 means O or S, R1 means alkyl containing one to six carbon atoms; R2 designates hydrogen or alkyl containing one to six carbon atoms; and R3 designates hydrogen or alkyl containing one to six carbon atoms substituted with the -ORa group where Ra means alkyl containing one to six carbon atoms; saturated nonaromatic cyclic radical containing 3 to 8 atoms in a cycle where one atom in a cycle is a heteroatom selected from N or O, whereas the rest of the atoms in the cycle are carbon atoms, one or two of these carbon atoms being not necessarily substituted by nitrogen atom with the groups -C(O)(C1-C6alcoxy) or -SO2-C1C6alkyl. Invention also relates to pharmaceutical composition.;EFFECT: compounds possess inhibiting activity.;13 cl, 1 tbl, 8 ex
机译:技术领域本发明涉及式I。<图像文件=“ 00000002.GIF” he =“ 27” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 54” />化合物或其药学上可接受的盐或水合物,其中Z表示N; X 1 表示O或S,R 1 表示含有1-6个碳原子的烷基; R 2 表示氢或含1-6个碳原子的烷基;和R 3 表示氢或含1-6个碳原子的-OR a 取代的烷基,其中R a 表示含1-6个烷基碳原子一个周期中包含3至8个原子的饱和非芳族环状自由基,其中一个原子是选自N或O的杂原子,而该周期中其余原子是碳原子,这些碳原子中的一个或两个不一定被氮原子取代的基团-C(O)(C 1 -C 6 烷氧基)或-SO 2 -C 1 C 6 烷基。本发明还涉及药物组合物;效果:具有抑制活性的化合物; 13 cl,1 tbl,8 ex

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