Departamento de Quimica Organica, Programa de Pos-Graduacao em Quimica, Outeiro de Sao Joao Batista,Universidade Federal Fluminense, s/n, Centro 24020-141 Niteroi-RJ, Brazil.
Departamento de Tecnologia Farmaceutica, aculdade de Farmacia, Universidade Federal Fluminense, F Rua Doutor Mario Viana, 523, Santa Rosa, 24241-000, Niteroi-RJ, Brazil.
Curr Org Synth. 2021 Oct 26;18(6):535-546. doi: 10.2174/1570179418666210224124603.
The subclass of compounds that have the nucleus 1, 4-naphthoquinone is the most diverse class of quinones, which have a large number of substances and have useful applications ranging from medicinal chemistry to application in materials with special properties. The introduction of one or two substituents with the sulfur heteroatom in the naphthoquinone nucleus generates products containing alkyl and aryl groups that amplify certain biological properties against bacteria, viruses, and fungi. There are several methods of preparing these compounds, mainly from low molecular weight naphthoquinones with two electrophilic sites capable of reacting with sulfides generating diversity and new classes of compounds, including new sulfur heterocycles and sulfur heterocycles fused with naphthoquinones. These compounds have been shown to be bioactive against several biological targets. This review will describe the methods of their synthesis and, when applicable, their biological activities.
具有 1,4-萘醌核的化合物子类是醌类中最多样化的一类,它们包含大量的物质,并且具有从药物化学到具有特殊性质的材料应用等广泛的用途。在萘醌核中引入一个或两个带有硫杂原子的取代基,会生成含有烷基和芳基的产物,从而增强对细菌、病毒和真菌的某些生物学特性。有几种方法可以制备这些化合物,主要是从具有两个可与硫化物反应的亲电位点的低分子量萘醌开始,从而产生多样性和新的化合物类别,包括新的硫杂环和与萘醌融合的硫杂环。这些化合物已被证明对多种生物靶标具有生物活性。本文将介绍它们的合成方法,以及在适用的情况下介绍其生物活性。