药物发现
背景(考古学)
组合化学
药品
脚手架
化学
纳米技术
计算生物学
计算机科学
药理学
生物
材料科学
生物化学
数据库
古生物学
作者
Tony Ge,Jean‐Christophe Cintrat
出处
期刊:Pharmaceuticals
[Multidisciplinary Digital Publishing Institute]
日期:2021-12-06
卷期号:14 (12): 1275-1275
被引量:2
摘要
Heterocyclic amino derivatives have been extensively synthesized and validated as potent bioactive compounds, and nowadays, numerous marketed drugs share these scaffolds, from very simple structures (monoamino, monocyclic compounds) to much more complex molecules (polycyclic derivatives with two or more nitrogen atoms within the (fused) rings). In a constant quest for new chemical entities in drug discovery, a few novel heterocycles have emerged in recent years as promising building blocks for the obtainment of bioactive modulators. In this context, pyrrolotriazinones have attracted attention, and some show promising biological activities. Here, we offer an extensive review of pyrrolo[2,1-f][1,2,4]triazin-4(1H)-one and pyrrolo[1,2-d][1,2,4]triazin-4(3H)-one, describing their biological properties en route to drug discovery.
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