Design, Synthesis, Antimicrobial, Anticancer, and Molecular Docking of Novel Quinoline Derivatives

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC
Kurls E. Anwer, Galal H. Sayed
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引用次数: 0

Abstract

A variety of novel pyrimidopyridoquinazoline, pyrazoloquinoline, and thiazoloquinoline derivatives were synthesized starting from 2,5,7-triamino-4-(4-methoxyphenyl)quinoline-3,8-dicarbonitrile under conventional heating. The same products were also prepared under microwave irradiation to improve the yield and time of the reactions. The structures of all newly synthesized compounds were proved by elemental analysis and IR, 1H and 13C NMR spectroscopy and mass spectrometry. The products were screened for their in vitro antimicrobial activity and showed moderate to high activity. They were also evaluated for anticancer activity against the HePG-2, HCT-116, and MCF-7 cell lines. Molecular docking was used to explore the molecular mechanism of the anticancer activity of 6-(4-methoxyphenyl)-3,9-dihydrodipyrazolo[3,4-b:3',4'-h]quinoline-1,5,7-triamine, which showed the highest cytotoxicity against all the test tested cancer cell lines.

Abstract Image

新型喹啉衍生物的设计、合成、抗菌、抗癌和分子对接
摘要 以2,5,7-三氨基-4-(4-甲氧基苯基)喹啉-3,8-二甲腈为原料,在常规加热条件下合成了多种新型嘧啶并喹唑啉、吡唑并喹啉和噻唑并喹啉衍生物。为了提高产率和缩短反应时间,还在微波辐照下制备了相同的产品。所有新合成化合物的结构均通过元素分析、红外光谱、1H 和 13C NMR 光谱以及质谱分析得到证实。对这些产品进行了体外抗菌活性筛选,结果显示它们具有中等到较高的活性。此外,还评估了它们对 HePG-2、HCT-116 和 MCF-7 细胞系的抗癌活性。分子对接法被用来探索 6-(4-甲氧基苯基)-3,9-二氢二吡唑并[3,4-b:3',4'-h]喹啉-1,5,7-三胺抗癌活性的分子机制,该化合物对所有测试的癌细胞株都显示出最高的细胞毒性。
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来源期刊
CiteScore
1.40
自引率
25.00%
发文量
139
审稿时长
3-6 weeks
期刊介绍: Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.
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