Synthesis and biological evaluation of 5-methyl-4-phenyl thiazole derivatives as anticancer agents
作者:Asaf E. Evren、Leyla Yurttas、Büşra Ekselli、Gülşen Akalin-Ciftci
DOI:10.1080/10426507.2018.1550642
日期:2019.8.3
Abstract New N-(5-methyl-4-phenylthiazol-2-yl)-2-(substituted thio)acetamides were synthesized and studied for their anticancer activity. The title compounds were procured by reacting 2-chloro-N-(5-methyl-4-phenylthiazol-2-yl)acetamide with some mercapto derivatives. The structural elucidation of the compounds was performed by 1H-NMR, 13C-NMR and LC-MS/MS spectral data and elemental analyses. The synthesized
摘要 合成了新的N-(5-甲基-4-苯基噻唑-2-基)-2-(取代硫基)乙酰胺并研究了它们的抗癌活性。通过使 2-氯-N-(5-甲基-4-苯基噻唑-2-基)乙酰胺与一些巯基衍生物反应获得标题化合物。通过1H-NMR、13C-NMR和LC-MS/MS光谱数据和元素分析对化合物进行结构解析。研究了合成的化合物对 A549 人肺腺癌细胞和 NIH/3T3 小鼠胚胎细胞系的抗肿瘤活性,以确定它们的选择性细胞毒性。2-[(1-methyl-1H-tetrazol-5-yl)thio]-N-(5-methyl-4-phenylthiazol-2-yl)acetamide (4c) 显示出高选择性,其 IC50 值为 23.30 ± 0.35 µM 和 > 1000 µM 分别针对 A549 人肺腺癌细胞和 NIH/3T3 小鼠胚胎母细胞系。2-[(1-甲基-1H-咪唑-2-基)硫代]-N-(5-甲基-