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天然产物环氧化酶 (COX) 抑制剂:现状与未来展望综述。

Natural Product Inhibitors of Cyclooxygenase (COX) Enzyme: A Review on Current Status and Future Perspectives.

机构信息

Department of Natural Products, National Institute of Pharmaceutical Education and Research (NIPER), Sector-67, SAS Nagar 160062, Mohali, India.

出版信息

Curr Med Chem. 2021;28(10):1877-1905. doi: 10.2174/0929867327666200602131100.

Abstract

BACKGROUND

Several clinically used COX-1 and COX-2 inhibitor drugs were reported to possess severe side effects like GI ulcers and cardiovascular disturbances, respectively. Natural products being structurally diverse always attracted the attention of chemists/ medicinal chemists as a potential source of lead molecules in the drug discovery process. COX-2 inhibitory natural products also possess potential cancer chemopreventive property against various cancers including that of colon, breast and prostate.

METHODS

Various in vitro, in vivo and in silico standardized methods were used to evaluate COX inhibition property of different secondary metabolites isolated from plant, microbial and marine origin.

RESULTS

We had earlier reported a detailed account of natural product inhibitors of COX reported during 1995-2005, in 2006. In the proposed review, we report 158 natural product inhibitors of COX during 2006 to 2019 belonging to various secondary metabolite classes such as alkaloids, terpenoids, polyphenols as flavonoids, chromones, coumarins, lignans, anthraquinones, naphthalenes, curcuminoids, diarylheptanoids and miscellaneous compounds of plant and marine origin. Further Structure Activity Relationship (SAR) studies of possible leads are also included in the article.

CONCLUSION

COX inhibitors served as a potential source of lead molecules for the discovery and development of anti-inflammatory drugs. Compilation of natural product and semisynthetic inhibitors of COX may serve as valuable information to the researchers who are looking for possible lead molecules from a natural source to conduct further preclinical and clinical studies.

摘要

背景

一些临床使用的 COX-1 和 COX-2 抑制剂药物分别被报道具有严重的副作用,如胃肠道溃疡和心血管紊乱。天然产物结构多样,一直吸引着化学家/药物化学家的注意,是药物发现过程中潜在的先导分子来源。COX-2 抑制性天然产物也具有针对各种癌症(包括结肠癌、乳腺癌和前列腺癌)的潜在癌症化学预防特性。

方法

使用各种体外、体内和计算机标准化方法来评估从植物、微生物和海洋来源分离的不同次生代谢物的 COX 抑制特性。

结果

我们在 2006 年早些时候曾报道过 1995-2005 年间报道的 COX 天然产物抑制剂的详细情况。在本综述中,我们报告了 2006 年至 2019 年期间属于各种次生代谢物类别的 158 种 COX 天然产物抑制剂,如生物碱、萜类、多酚类(如黄酮类、色酮类、香豆素类、木脂素类、蒽醌类、萘类、姜黄素类、二芳基庚烷类和植物及海洋来源的其他化合物)。还包括了可能的先导化合物的结构活性关系(SAR)研究。

结论

COX 抑制剂是发现和开发抗炎药物的潜在先导分子来源。COX 的天然产物和半合成抑制剂的编目可为那些希望从天然来源寻找可能的先导分子以进行进一步的临床前和临床研究的研究人员提供有价值的信息。

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