首页> 外国专利> - 1h-inol-2 carboxilic extracted from (phenyl) acid 7 - (isocyclic-1-methyl) amide as p38 MAP quinasa inhibitor

- 1h-inol-2 carboxilic extracted from (phenyl) acid 7 - (isocyclic-1-methyl) amide as p38 MAP quinasa inhibitor

机译:-从(苯基)酸7中提取1h-inol-2羧酸-作为p38 MAP quinasa抑制剂的(异环-1-甲基)酰胺

摘要

For a formula compound I, AR is preferably 5-tercbutil-3-metalansulfonilamino-2-methoxy-fenil; R1 is cyclo-c4-c6, may have 1-2n cyclopentadiene, may have monomer or substitute R7; R7 is tar of C1-C3, hydroxyl, C1-C3, amino, etc.; R2 h, halide, C1 tar; MES ch, N; t is link, C1-C4 or c10-c3 not replaced. N is 1-3 P is 0-3 The most popular compounds are: (5-terc-butil-3-metalansulfonilamino-2-methoxi-fenil) - 1-methyl-7 - [4 - (1-methyl-piperidin-4-carbon) - piperazin-1-ilmethyl] - 1h-indol-2-carboxilico;[5-terc-butil-2-methoxi-3 - (4-methyl-piperazin-1-ilmet) - fenil] - Amida del acido (s) - 1-meth-7 - [4 - (1-meth-pirrolidin-2-carboxil) - piperazin-1-ilmet] - 1h-indol-2-carboxillico; among others. A pharmaceutical composer was also mentioned These compounds are effective inhibitors of map quinasa p38 in the treatment of respiratory diseases.
机译:对于式I化合物,AR优选为5-tercbutil-3-金属磺酰基氨基-2-甲氧基-苯腈; R1为环-c4-c6,可具有1-2n的环戊二烯,可具有单体或取代基R7; R 7是C 1 -C 3的焦油,羟基,C 1 -C 3,氨基等。 R 2 h,卤化物,C 1焦油; MES ch,N; t是链接,未替换C1-C4或c10-c3。 N是1-3 P是0-3最受欢迎的化合物是:(5-terc-butil-3-metalansulfonilamino-2-methoxi-fenil)-1-methyl-7-[4--(1-methyl-piperidin- 4-碳)-哌嗪-1-基甲基]-1h-吲哚-2-羧;(5-terc-butil-2-methoxi-3-(4-甲基-哌嗪-1-基)-fenil]-阿米达acido(s)-1-meth-7-[4--(1-meth-pirrolidin-2-carboxil)-piperazin-1-ilmet]-1h-indol-2-carboxillico;其中。还提到了药物组合物。这些化合物在呼吸道疾病的治疗中是map quinasa p38的有效抑制剂。

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