异氰
化学
药效团
抗真菌
药物发现
组合化学
药物化学
立体化学
生物化学
微生物学
生物
作者
Alberto Massarotti,Francesca Brunelli,Silvio Aprile,Mariateresa Giustiniano,Gian Cesare Tron
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2021-07-01
卷期号:121 (17): 10742-10788
被引量:105
标识
DOI:10.1021/acs.chemrev.1c00143
摘要
In eons of evolution, isocyanides carved out a niche in the ecological systems probably thanks to their metal coordinating properties. In 1859 the first isocyanide was synthesized by humans and in 1950 the first natural isocyanide was discovered. Now, at the beginning of XXI century, hundreds of isocyanides have been isolated both in prokaryotes and eukaryotes and thousands have been synthesized in the laboratory. For some of them their ecological role is known, and their potent biological activity as antibacterial, antifungal, antimalarial, antifouling, and antitumoral compounds has been described. Notwithstanding, the isocyanides have not gained a good reputation among medicinal chemists who have erroneously considered them either too reactive or metabolically unstable, and this has restricted their main use to technical applications as ligands in coordination chemistry. The aim of this review is therefore to show the richness in biological activity of the isocyanide-containing molecules, to support the idea of using the isocyanide functional group as an unconventional pharmacophore especially useful as a metal coordinating warhead. The unhidden hope is to convince the skeptical medicinal chemists of the isocyanide potential in many areas of drug discovery and considering them in the design of future drugs.
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