Department of Organic Chemistry, Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St., Moscow 117198, Russia.
Department of Pharmacy-Drug Sciences, University of Bari Aldo Moro, Via E. Orabona 4, 70125 Bari, Italy.
Future Med Chem. 2019 Oct;11(20):2735-2755. doi: 10.4155/fmc-2019-0136. Epub 2019 Sep 26.
Pyrrolo[2,1-]isoquinoline (PIq) is a nitrogen heterocyclic scaffold of diverse alkaloids endowed with several biological activities, including antiretroviral and antitumor activities. Several 5,6-dihydro-PIq (DHPIq) alkaloids, belonging to the lamellarins' family, have proved to be cytotoxic to tumor cells, as well as reversers of multidrug resistance. In this review, we provide an overview of the main achievements over the last decade in the synthetic approaches to access libraries of PIq compounds along with a survey, as comprehensive as possible, of bioactivity, mechanism of action, pharmacophore and structure-activity relationships of synthetic analogs of DHPIq-based alkaloids. The focus is mainly on the potential exploitation of the (DH)PIq scaffold in design and development of novel antitumor drugs.
吡咯并[2,1-]异喹啉(PIq)是一种具有多种生物活性的含氮杂环骨架,包括抗逆转录病毒和抗肿瘤活性。几种 5,6-二氢-PIq(DHPIq)生物碱属于 lamellarins 家族,已被证明对肿瘤细胞具有细胞毒性,并且可以逆转多药耐药性。在这篇综述中,我们概述了过去十年中在合成 PIq 化合物库的方法方面的主要成就,并尽可能全面地调查了基于 DHPIq 生物碱的合成类似物的生物活性、作用机制、药效团和构效关系。重点主要是在设计和开发新型抗肿瘤药物方面对(DH)PIq 支架的潜在利用。