首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >DESIGN, SYNTHESIS, IN VITRO ANTIPROLIFERATIVE ACTIVITY EVALUATION OF 2-ALICANOYLAMIDOTHIOPHENE-3-CARBOXAMIDE DERIVATIVES
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DESIGN, SYNTHESIS, IN VITRO ANTIPROLIFERATIVE ACTIVITY EVALUATION OF 2-ALICANOYLAMIDOTHIOPHENE-3-CARBOXAMIDE DERIVATIVES

机译:设计,合成,体外抗2-丙氨酰氨基噻吩并菲-3-羧酰胺衍生物的活性评估

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摘要

A series of 2-alkanoylamidothiophene-3-carboxamide derivatives were synthesized based on the hit compound 1. The anti-proliferative activity of all the compounds in vitro against MGC-803 (stomach) and HCT-116 (colon) cancer cell lines using SRB assays were tested. Several compounds showed improved anti-proliferative activity against MGC-803 and HCT-116. SAR study revealed that chlorine substituent in the 2-acetylamino part was important for anti-proliferative activity. 5a, 11b, 11c and lid were the most potent compounds against MGC-803 (IC(50)s = 2.32-2.95 mu M), and 5a and 11c also showed good anti-proliferative activity against HCT-116 cells (IC(50)s = 3.41-3.75 mu M). In addition, the anti-proliferative activity of llb and lid could be attributed to the apoptosis in HCT116 cells via caspase 3 activation, confirmed by flow cytometry assay and western blot analysis. Meanwhile, lib and lid decreased the mitochondrial membrane potential (MMP) in HCT116 cells.
机译:基于命中化合物1合成了一系列2-链烷酰胺基噻吩-3-甲酰胺衍生物。使用SRB,所有化合物在体外对MGC-803(胃)和HCT-116(结肠)癌细胞系的抗增殖活性。测试了测试。几种化合物显示出针对MGC-803和HCT-116的增强的抗增殖活性。 SAR研究表明,2-乙酰氨基部分中的氯取代基对于抗增殖活性很重要。 5a,11b,11c和盖是对抗MGC-803的最有效化合物(IC(50)s = 2.32-2.95μM),而5a和11c也显示出对HCT-116细胞的良好抗增殖活性(IC(50 s =3.41-3.75μM)。此外,流式细胞仪和western blot分析证实,IIb和IId的抗增殖活性可归因于caspase 3激活导致HCT116细胞凋亡。同时,lib和lid降低了HCT116细胞的线粒体膜电位(MMP)。

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