芳基
结构母题
功能(生物学)
化学
组合化学
计算生物学
生物化学
生物
有机化学
遗传学
烷基
作者
Maura Marinozzi,Gloria Marcelli,Andrea Carotti
出处
期刊:Mini-reviews in Medicinal Chemistry
[Bentham Science]
日期:2015-03-26
卷期号:15 (4): 272-299
被引量:23
标识
DOI:10.2174/1389557515666150312154536
摘要
N-Aryl-5-aminopyrazole represents a key structural motif in a plethora of biologically active molecules endowed with a wide spectrum of pharmacological properties. Accordingly, this scaffold can be certainly included in the category of a privileged structure. As an example, N-aryl-5- aminopyrazole along with its 5-ureido derivatives are recurrent scaffolds in the field of inhibition of the different members of mitogen-activated protein kinases (MAPKs). Over the past recent years a large number of papers highlighting the design, synthesis and biological evaluation of different classes of N-aryl-5-aminopyrazole-containing compounds have been reported in the literature, but a review on this topic is still missing. With the aim to fill this gap, the present review article focuses on the recent developments (1995-mid2014) on the application of the N-aryl-5-aminopyrazole-based compounds in different therapeutic fields, with a particular attention to the design and structure-activity relationships (SAR) aspects of each class of compounds. Keywords: Biologically active compounds, nitrogen-heterocycle, pyrazole, privileged structure.
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