Recent Developments on the Synthesis and Biological Activities of Fused Pyrimidinone Derivatives

被引:15
|
作者
Seboletswe, Pule [1 ]
Awolade, Paul [1 ]
Singh, Parvesh [1 ]
机构
[1] Univ KwaZulu Natal, Sch Chem & Phys, Private Bag X01, Durban, South Africa
基金
新加坡国家研究基金会;
关键词
Heterocycles; fused pyrimidinones; organic synthesis; medicinal chemistry; biological activities; ANTIBACTERIAL ACTIVITY; ANTICANCER; HYBRIDS; DESIGN; CYTOTOXICITY; HETEROCYCLES; CHEMISTRY; DOCKING; SAR;
D O I
10.1002/cmdc.202100083
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Heterocyclic compounds constitute a unique class of organic compounds endowed with a wide range of synthetic and pharmaceutical applications. Pyrimidinones and their fused analogues have received focused attention in this regard, partly due to their mimicry of nucleobases which consequently forges their interesting medicinal properties. Over the years, the medicinal chemistry research community has experienced an upsurge in articles describing the exploration of these scaffolds to develop effective therapeutic agents. Several biological activities, including antimicrobial, antiviral, anticancer, antidiabetic, anti-inflammatory, anticonvulsive, and antihistaminic, have been well documented. This minireview presents a compendium of recent developments (2017-2020) focused on the synthesis and biological activities of fused pyrimidinones. The goal is to update medicinal chemists on the therapeutic relevance of fused pyrimidinones and the molecular architecture of clinic-worthy drug candidates. A brief account of the structure-activity relationships (SAR) revealed from different biological assays is also discussed.
引用
收藏
页码:2050 / 2067
页数:18
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