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从植物源萜类内酯骨架中开发潜在的抗肿瘤药物。

Development of Potential Antitumor Agents from the Scaffolds of Plant-Derived Terpenoid Lactones.

机构信息

Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, United States.

出版信息

J Med Chem. 2020 Dec 24;63(24):15410-15448. doi: 10.1021/acs.jmedchem.0c01449. Epub 2020 Dec 8.

Abstract

Naturally occurring terpenoid lactones and their synthetic derivatives have attracted increasing interest for their promising antitumor activity and potential utilization in the discovery and design of new antitumor agents. In the present perspective article, selected plant-derived five-membered γ-lactones and six-membered δ-lactones that occur with terpenoid scaffolds are reviewed, with their structures, cancer cell line cytotoxicity and in vivo antitumor activity, structure-activity relationships, mechanism of action, and the potential for developing cancer chemotherapeutic agents discussed in each case. The compounds presented include artemisinin (ART, ), parthenolide (PTL, ), thapsigargin (TPG, ), andrographolide (AGL, ), ginkgolide B (GKL B, ), jolkinolide B (JKL B, ), nagilactone E (NGL E, ), triptolide (TPL, ), bruceantin (BRC, ), dichapetalin A (DCT A, ), and limonin (LMN, ), and their naturally occurring analogues and synthetic derivatives. It is hoped that this contribution will be supportive of the future development of additional efficacious anticancer agents derived from natural products.

摘要

天然萜类内酯及其合成衍生物因其有希望的抗肿瘤活性和在发现和设计新型抗肿瘤药物方面的潜在应用而引起了越来越多的关注。在本综述文章中,对具有萜类骨架的植物来源的五元γ-内酯和六元δ-内酯进行了综述,讨论了它们的结构、癌细胞系细胞毒性和体内抗肿瘤活性、构效关系、作用机制以及开发癌症化疗药物的潜力。所介绍的化合物包括青蒿素(ART, )、紫草酸内酯(PTL, )、他普汀(TPG, )、穿心莲内酯(AGL, )、银杏内酯 B(GKL B, )、吉枯螺内酯 B(JKL B, )、那格列酮 E(NGL E, )、雷公藤红素(TPL, )、布鲁斯汀(BRC, )、二氢卡帕他丁 A(DCT A, )和柠檬苦素(LMN, )及其天然类似物和合成衍生物。希望这篇综述能够支持未来从天然产物中开发出更多有效的抗癌药物。

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