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Synthesis and biological evaluation of novel dabigatran derivatives as thrombin inhibitors

机译:新型达比加群衍生物作为凝血酶抑制剂的合成及生物学评价

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摘要

A novel series of 3-[{2-[(4-carbamimidoylphenylamino)methyl]-1-substituted-1H-benzoimidazole-5-carbonyl}(3-chloro-4-fluorophenyl)amino]propionic derivatives of dabigatran was synthesized. The structures of the compounds were characterized by H-1 NMR, C-13 NMR, HRMS, and elemental analysis. The compounds were screened for in vitro thrombin inhibitory activity. The results indicated that the compounds had low to moderate inhibitory activity. The compounds with N-methyl and N-ethyl side chains had much greater inhibitory activity against thrombin than those with other side chains.
机译:合成了达比加群的3-[{{2-[(4-氨基甲酰基苯基氨基)甲基] -1-取代的-1H-苯并咪唑-5-羰基}(3-氯-4-氟苯基)氨基]丙酸衍生物系列。化合物的结构通过H-1 NMR,C-13 NMR,HRMS和元素分析进行​​表征。筛选化合物的体外凝血酶抑制活性。结果表明该化合物具有低至中等的抑制活性。具有N-甲基和N-乙基侧链的化合物对凝血酶的抑制活性比具有其他侧链的化合物大。

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