从洋葱皮废弃物中探寻抗癌分子;罕见槲皮素衍生物--Pachypodol 的首次合成与生物学研究

Q2 Pharmacology, Toxicology and Pharmaceutics
Pandurangan Nanjan, Jyotsna Nambiar, Chinchu Bose, Asoke Banerji, Bipin G. Nair
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引用次数: 0

摘要

随着全球洋葱产量的不断增加,洋葱皮废物的产生量也随之增加。其难闻的气味使其无法用于农业或进行处理,因为填埋会带来环境问题。以前的研究表明,洋葱废弃物中含有两种主要的黄酮类化合物,即槲皮素及其苷(螺旋苷)。通过利用螺旋苷(槲皮素-4ʹ-葡萄糖苷),已开发并实现了一种阿育吠陀药用必需品--Pachypodol(槲皮素-3,3′,7-三甲基醚和一种稀有黄酮醇)的快速合成。研究了 Pachypodol 及其类似物抑制基质金属蛋白酶-2 和-9(MMP-2 和 9)活性的能力。硅内对接研究表明,与大多数已知的 MMP 抑制剂不同,Pachypodol 通过 Ile222、Tyr223 和 Thr227 残基选择性地与 MMP-2 发生锌依赖性反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Probing Anticancer Molecules from Onion Peels Waste; First Synthesis and Biological Studies of a Rare Quercetin Derivative-Pachypodol
The constant increase in global onion production escalates the generation of onion peel waste. For instance, globally, >50 lakh tons of onion waste are generated annually. Its objectionable odor precludes its use in agriculture or disposal as landfilling presents environmental issues. Previous studies show that two major flavonoids, quercetin and its glycosides (spiraeoside), have been identified in abundance in onion waste. By utilizing the spiraeoside (quercetin-4ʹ-glucoside), a rapid synthesis of pachypodol (quercetin-3,3′,7-trimethyl ether, and a rare flavonol), an essential Ayurvedic product, has been developed and achieved. Pachypodol and analogs were studied for their ability to inhibit matrix metalloproteinase-2 and -9 (MMP-2 & 9) activity. Amongst the compounds tested, pachypodol significantly inhibited MMP-2 activity. In-silico docking studies suggest that, unlike most known MMP inhibitors, pachypodol interacts selectively with MMP-2 through the residues Ile222, Tyr223, and Thr227 in a zincindependent manner. The experimental studies also prove that pachypodol inhibits the MMP-2 enzyme in a zinc-independent way.
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来源期刊
Current Bioactive Compounds
Current Bioactive Compounds Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.90
自引率
0.00%
发文量
112
期刊介绍: The journal aims to provide comprehensive review articles on new bioactive compounds with proven activities in various biological screenings and pharmacological models with a special emphasis on stereoeselective synthesis. The aim is to provide a valuable information source of bioactive compounds synthesized or isolated, which can be used for further development of pharmaceuticals by industry and academia. The journal should prove to be essential reading for pharmacologists, natural product chemists and medicinal chemists who wish to be kept informed and up-to-date with the most important developments on new bioactive compounds of natural or synthetic origin, including their stereoeselective synthesis.
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