首页> 外国专利> SYNTHESIS AND BIOLOGICAL EVALUATION OF 2',5'-DIMETHOXYCHALCONE DERIVATIVES AS MICROTUBULE-TARGETED ANTICANCER AGENTS

SYNTHESIS AND BIOLOGICAL EVALUATION OF 2',5'-DIMETHOXYCHALCONE DERIVATIVES AS MICROTUBULE-TARGETED ANTICANCER AGENTS

机译:2',5'-二甲氧基查尔酮衍生物作为微管靶向抗癌剂的合成及生物学评价

摘要

Disclosed are a serious of 2′,5′-dimethoxychalcone derivatives for treating cancer, wherein 2,5-dimethoxyacetophenone and methyl 4-formylbenzoate are condensed to form 4-carboxyl-2′,5′-dimethoxychalcone (compound 1), which is further reacted with alkyl halides or amines to synthesize the chalcone derivatives of compounds 2-17. In addition, 2,5-dimethoxyacetophenone is reacted with 5-formyl-2-thiophenecarboxylic acid to form compound 18 (3-(3-thiophene)carboxyl-1-(2,5-dimethoxyphenyl)prop-2-en-1-one). The synthesized 2′,5′-dimethoxychalcone derivatives can be acted as microtubule-targeted tubulin-polymerizing agents.
机译:公开了一种用于治疗癌症的严重的2',5'-二甲氧基查耳酮衍生物,其中2,5-二甲氧基苯乙酮和4-甲酰基苯甲酸甲酯缩合形成4-羧基-2',5'-二甲氧基查耳酮(化合物1),进一步与烷基卤化物或胺反应以合成化合物2-17的查耳酮衍生物。另外,使2,5-二甲氧基苯乙酮与5-甲酰基-2-噻吩羧酸反应形成化合物18(3-(3-噻吩)羧基-1-(2,5-二甲氧基苯基)丙-2-烯-1-一)。合成的2',5'-二甲氧基查耳酮衍生物可以用作靶向微管的微管蛋白聚合剂。

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