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小檗碱9-苯甲酸衍生物的合成及其抗氧化活性

Synthesis and antioxidant activities of berberine 9--benzoic acid derivatives.

作者信息

Liu Yanfei, Long Shuo, Zhang Shanshan, Tan Yifu, Wang Ting, Wu Yuwei, Jiang Ting, Liu Xiaoqin, Peng Dongming, Liu Zhenbao

机构信息

Department of Pharmaceutical Engineering, College of Chemistry and Chemical Engineering, Central South University Changsha 410083 China.

Department of Pharmaceutics, Xiangya School of Pharmaceutical Sciences, Central South University Changsha 410013 China

出版信息

RSC Adv. 2021 May 13;11(29):17611-17621. doi: 10.1039/d1ra01339d.

Abstract

Although berberine (BBR) shows antioxidant activity, its activity is limited. We synthesized 9--benzoic acid berberine derivatives, and their antioxidant activities were screened ABTS, DPPH, HOSC and FRAP assays. The -position was modified with halogen elements on the benzoic acid ring, which led to an enhanced antioxidant activity and the substituent on the -position was found to be better than the -position. Compounds 8p, 8c, 8d, 8i, 8j, 8l, and especially 8p showed significantly higher antioxidant activities, which could be attributed to the electronic donating groups. All the berberine derivatives possessed proper lipophilicities. In conclusion, compound 8p is a promising antioxidant candidate with remarkable elevated antioxidant activity and moderate lipophilicity.

摘要

虽然黄连素(BBR)具有抗氧化活性,但其活性有限。我们合成了9-苯甲酸黄连素衍生物,并通过ABTS、DPPH、HOSC和FRAP测定法筛选了它们的抗氧化活性。在苯甲酸环上用卤素元素修饰了α-位,这导致抗氧化活性增强,并且发现α-位上的取代基比β-位更好。化合物8p、8c、8d、8i、8j、8l,尤其是8p表现出显著更高的抗氧化活性,这可能归因于供电子基团。所有黄连素衍生物都具有适当的亲脂性。总之,化合物8p是一种有前途的抗氧化剂候选物,具有显著提高的抗氧化活性和适度的亲脂性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8673/9033176/ec617b1a9815/d1ra01339d-s1.jpg

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