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作为直接多靶点配体的杂合化合物:综述

Hybrid Compounds as Direct Multitarget Ligands: A Review.

作者信息

de Oliveira Pedrosa Michelle, Duarte da Cruz Rayssa Marques, de Oliveira Viana Jessika, de Moura Ricardo Olimpio, Ishiki Hamilton Mitsugu, Barbosa Filho Jose Maria, Diniz Margareth F F M, Scotti Marcus Tullius, Scotti Luciana, Bezerra Mendonca Francisco Jaime

机构信息

Laboratory of Synthesis and Drug Delivery, Department of Biological Science, State University of Paraiba, Joao Pessoa, PB,. Brazil.

University of Western Sao Paulo (Unoeste), Presidente Prudente, SP,. Brazil.

出版信息

Curr Top Med Chem. 2017;17(9):1044-1079. doi: 10.2174/1568026616666160927160620.

Abstract

Molecular Hybridization is an approach in rational drug design where new chemical entities are obtained by combining two or more pharmacophoric units from different bioactive compounds into a single molecule. Through this approach, medicinal chemists hope that the new hybrid derivative presents: better affinity and efficacy when compared to the parent drugs; a modified selectivity profile with improvement over pharmacokinetic and pharmacodynamic restrictions; dual or multiple modes of action; reduction of undesirable side effects; decreases in drug-drug interactions; reduced emergence or spread of drug resistance in microorganisms and protozoans; and lower cost. The approach has been successfully used by many research groups around the world and has had very promising results with diseases having multifactorial profiles, like Alzheimer´s, Parkinson´s disease, cancer, inflammation, and hypertension among others. The purpose of this paper is to conduct an updated review of molecular hybridization and multitarget profiling (a rational drug design approach), and its applications to the design and discovery of novel hybrid compounds with anti-inflammatory, antimicrobial, anticancer and antiprotozoal (leishmaniasis, malaria, and schistosomiasis) activities over the last six years.

摘要

分子杂交是合理药物设计中的一种方法,即通过将来自不同生物活性化合物的两个或更多药效基团单元组合到一个分子中,从而获得新的化学实体。通过这种方法,药物化学家希望新的杂交衍生物具有以下特点:与母体药物相比,具有更好的亲和力和疗效;具有经过改良的选择性,在药代动力学和药效学限制方面有所改善;具有双重或多种作用模式;减少不良副作用;减少药物相互作用;降低微生物和原生动物中耐药性的出现或传播;以及降低成本。该方法已被世界各地的许多研究小组成功使用,并在具有多因素特征的疾病(如阿尔茨海默病、帕金森病、癌症、炎症和高血压等)方面取得了非常有前景的成果。本文的目的是对分子杂交和多靶点分析(一种合理药物设计方法)进行更新综述,并阐述其在过去六年中在设计和发现具有抗炎、抗菌、抗癌和抗原虫(利什曼病、疟疾和血吸虫病)活性的新型杂交化合物方面的应用。

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