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Synthesis and Anticancer Activity of 3,4,5-Trimethoxycinnamamide-Tethered 1,2,3-Triazole Derivatives
Russian Journal of Organic Chemistry ( IF 0.8 ) Pub Date : 2022-03-01 , DOI: 10.1134/s1070428022010122 A. Sanjeev , N. N. Reddy , S. Bhaskar , R. Rohini , A. K. Raju , B. V. Kumar , A. Hu , P. M. Reddy
中文翻译:
3,4,5-三甲氧基肉桂酰胺-栓系1,2,3-三唑衍生物的合成及抗癌活性
更新日期:2022-03-01
Russian Journal of Organic Chemistry ( IF 0.8 ) Pub Date : 2022-03-01 , DOI: 10.1134/s1070428022010122 A. Sanjeev , N. N. Reddy , S. Bhaskar , R. Rohini , A. K. Raju , B. V. Kumar , A. Hu , P. M. Reddy
Abstract
A series of novel 3,4,5-trimethoxycinnamamide-tethered 1,2,3-triazole derivatives were prepared by the click reaction of (E)-N-(prop-2-yn-1-yl)-3-(3,4,5-trimethoxyphenyl) acrylamide with different aryl azides. The synthesized compounds were characterized by 1H and 13C NMR and mass spectra and elemental analyses and were screened for their in vitro anticancer activity against MCF-7 and A549 cell lines by using MTT assay. Most of the tested compounds showed prominent activity against both cancer cell lines.
中文翻译:
3,4,5-三甲氧基肉桂酰胺-栓系1,2,3-三唑衍生物的合成及抗癌活性
摘要
( E ) -N- (prop-2-yn-1-yl)-3-(3 ,4,5-三甲氧基苯基)丙烯酰胺与不同的芳基叠氮化物。合成的化合物通过1 H 和13 C NMR 以及质谱和元素分析进行表征,并通过 MTT 法筛选它们对 MCF-7 和 A549 细胞系的体外抗癌活性。大多数测试的化合物对两种癌细胞系都显示出显着的活性。