Design, Synthesis and Anticancer Activity of Novel Substituted (E)-2-Morpholinoquinoline- 3-carbaldehyde-O-((-1-aryl-1H-1,2,3-triazol-4-yl)methyl)oxime Derivatives

Q4 Chemistry
Aruna Jyothi Chatla, J. Yerrabelly, Nagaraju Dharavath, Panga Shyam
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引用次数: 0

Abstract

A new series of substituted (E)-2-morpholinoquinoline-3-carbaldehyde-O-((-1-phenyl-1H-1,2,3-triazol-4-yl)methyl)oxime scaffolds were synthesized from involving alkynyl quinoline oximes with various aryl azides by click reaction obtained corresponding compounds with high yields. The synthesized compounds were characterized by using IR, 1H NMR, 13C NMR and HRMS data. All the synthesized compounds screened anticancer activity against MCF-7, HeLa, PC-3 cell lines. All the compounds exhibited good results among them 8b, 8g and 8i compounds have shown prominent anticancer activity are compared to standard drug doxorubicin.
新型取代(E)-2-吗啉基喹啉-3-甲醛-O-((-1-芳基-1H-1,2,3-三唑-4-基)甲基)肟衍生物的设计、合成和抗癌活性
本研究以炔基喹啉肟与各种芳基叠氮化物为原料,通过点击反应合成了一系列新的取代(E)-2-吗啉基喹啉-3-甲醛-O-((-1-苯基-1H-1,2,3-三唑-4-基)甲基)肟支架,并以高产率获得了相应的化合物。利用红外光谱、1H NMR、13C NMR 和 HRMS 数据对合成的化合物进行了表征。所有合成化合物都对 MCF-7、HeLa 和 PC-3 细胞系进行了抗癌活性筛选。与标准药物多柔比星相比,所有化合物都表现出了良好的抗癌活性,其中 8b、8g 和 8i 化合物的抗癌活性更为突出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Asian Journal of Chemistry
Asian Journal of Chemistry 化学-化学综合
CiteScore
0.80
自引率
0.00%
发文量
229
审稿时长
4 months
期刊介绍: Information not localized
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