嘌呤
化学
嘧啶
咪唑
组合化学
嘌呤类似物
部分
嘌呤代谢
立体化学
有机化学
酶
作者
Soukaina Benkirane,Houria Misbahi,Meriem Boudkhili,Youssef Kandri Rodi,Nada Kheira Sebbar,El Mokhtar Essassi
标识
DOI:10.2174/0113852728260602231018040338
摘要
Abstract: The Purine moiety is regarded as the ubiquitous nitrogen-containing heterocycle in nature and is recognized as a privileged scaffold in medicinal chemistry. Moreover, the purine derivatives are heterocyclic aromatic compounds consisting of conjoined pyrimidine and imidazole moieties. Purine derivatives are involved in various metabolic processes as cofactors associated with a wide variety of enzymes and receptors. Therefore, many synthetic ways to obtain purine derivatives were developed using different reagents such as pyrimidine, imidazole, and some acyclic precursors. This article review focuses on the synthetic methodologies of purine derivatives from its first synthesis in the 19th century to this last decade and also reports a variety of proven pharmacological applications for the purine derivatives. This review offers a panoply of synthetic routes that medicinal and organic chemistry researchers can use in the preparation and design of new purine derivatives.
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