恶唑
化学
组合化学
药物发现
药理学
立体化学
计算生物学
生物化学
生物
作者
Maria Assunta Chiacchio,Giuseppe Lanza,Ugo Chiacchio,Salvatore V. Giofrè,Roberto Romeo,Daniela Iannazzo,Laura Legnani
标识
DOI:10.2174/0929867326666181203130402
摘要
Heterocyclic compounds represent a significant target for anti-cancer research and drug discovery, due to their structural and chemical diversity. Oxazoles, with oxygen and nitrogen atoms present in the core structure, enable various types of interactions with different enzymes and receptors, favoring the discovery of new drugs. Aim of this review is to describe the most recent reports on the use of oxazole-based compounds in anticancer research, with reference to the newly discovered iso/oxazole-based drugs, to their synthesis and to the evaluation of the most biologically active derivatives. The corresponding dehydrogenated derivatives, i.e. iso/oxazolines and iso/oxazolidines, are also reported.
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