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生物碱作为抗癌药物发现中的环氧化酶抑制剂

Alkaloids as Cyclooxygenase Inhibitors in Anticancer Drug Discovery.

作者信息

Hashmi Muhammad Ali, Khan Afsar, Farooq Umar, Khan Sehroon

机构信息

Department of Chemistry, COMSATS Institute of Information Technology, Abbottabad-22060. Pakistan.

Key Laboratory of Economic Plants and Biotechnology, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 560201, Yunnan. China.

出版信息

Curr Protein Pept Sci. 2018;19(3):292-301. doi: 10.2174/1389203718666170106103031.

Abstract

Cancer is the leading cause of death worldwide and anticancer drug discovery is a very hot area of research at present. There are various factors which control and affect cancer, out of which enzymes like cyclooxygenase-2 (COX-2) play a vital role in the growth of tumor cells. Inhibition of this enzyme is a very useful target for the prevention of various types of cancers. Alkaloids are a diverse group of naturally occurring compounds which have shown great COX-2 inhibitory activity both in vitro and in vivo. In this mini-review, we have discussed different alkaloids with COX-2 inhibitory activities and anticancer potential which may act as leads in modern anticancer drug discovery. Different classes of alkaloids including isoquinoline alkaloids, indole alkaloids, piperidine alkaloids, quinazoline alkaloids, and various miscellaneous alkaloids obtained from natural sources have been discussed in detail in this review.

摘要

癌症是全球主要死因,目前抗癌药物研发是一个非常热门的研究领域。有多种因素控制和影响癌症,其中环氧化酶-2(COX-2)等酶在肿瘤细胞生长中起着至关重要的作用。抑制这种酶是预防各类癌症的一个非常有用的靶点。生物碱是一类多样的天然存在的化合物,在体外和体内均显示出强大的COX-2抑制活性。在本综述中,我们讨论了具有COX-2抑制活性和抗癌潜力的不同生物碱,它们可能成为现代抗癌药物研发的先导物。本综述详细讨论了不同类别的生物碱,包括异喹啉生物碱、吲哚生物碱、哌啶生物碱、喹唑啉生物碱以及从天然来源获得的各种其他生物碱。

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