受 Schizocommunin 启发的杂环混合分子

IF 1.4 4区 化学 Q3 CHEMISTRY, ORGANIC
Bhawna Chechani, Mukesh Kumar, Dinesh K. Yadav, Siddharth Sharma, Neetu Kumari
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引用次数: 0

摘要

本研究详细介绍了一种基于五味子素合成杂化分子的有效而环保的技术。这一过程包括利用喹唑啉酮、异atin 和叠氮化物进行点击反应。五味子素是一种天然生物活性化合物,具有广泛的生物功能,包括抗癌特性。由此产生的源于五味子黄素的三唑类化合物对三种人类癌细胞系的潜在抗癌活性进行了全面评估:通过 MTT 试验,对 MCF-7(乳腺癌)、A549(肺癌)和 PC-3(前列腺癌)这三种人类癌细胞株的潜在抗癌活性进行了全面评估。该系列中的一个化合物对 MCF-7 具有显著的抗癌效果(IC50 2.35 ± 0.67 μM)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Schizocommunin-inspired heterocyclic hybrid molecules

Schizocommunin-inspired heterocyclic hybrid molecules

An effective and environmentally friendly technique for synthesizing hybrid molecules based on schizocommunin has been detailed in this study. This process involves a click reaction utilizing quinazolinones, isatin, and azides. Schizocommunin, a natural bioactive compound recognized for its wide array of biological functions including its anticancer properties, was employed as the foundational scaffold. The resultant triazo compounds originating from schizocommunin were subjected to thorough evaluation for their potential anticancer activity against three human cancer cell lines: MCF-7 (breast cancer), A549 (lung cancer), and PC-3 (prostate cancer), through employment of the MTT assay. One compound from the series showcased a remarkable anticancer efficacy (IC50 2.35 ± 0.67 μM) against MCF-7.

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来源期刊
CiteScore
2.90
自引率
13.30%
发文量
98
审稿时长
1 months
期刊介绍: The international journal Chemistry of Heterocyclic Compounds publishes original papers, short communications, reviews, and mini-reviews dealing with problems in the field of heterocyclic chemistry in Russian and English. The Journal also publishes reviews and annotations on new books and brief reports on conferences in the field of heterocyclic chemistry, as well as commemo­ra­tives dedicated to prominent heterocyclic chemists.
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