Medicinal Chemistry of Isocyanides

被引:106
作者
Massarotti, Alberto [1 ]
Brunelli, Francesca [1 ]
Aprile, Silvio [1 ]
Giustiniano, Mariateresa [2 ]
Tron, Gian Cesare [1 ]
机构
[1] Univ Piemonte Orientale, Dipartimento Sci Farmaco, I-28100 Novara, Italy
[2] Univ Napoli Federico II, Dipartimento Farm, I-80131 Naples, Italy
关键词
BIOACTIVE MARINE METABOLITES; ANTI-BARNACLE ACTIVITY; BON BAIN-AGGR; DITERPENE ISONITRILES; NITROGENOUS SESQUITERPENES; AMINO-ACIDS; ANTIMALARIAL ACTIVITY; ANTIFOULING ACTIVITY; TRICHODERMA-HAMATUM; ETHYL ISOCYANIDE;
D O I
10.1021/acs.chemrev.1c00143
中图分类号
O6 [化学];
学科分类号
0703 ;
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.
引用
收藏
页码:10742 / 10788
页数:47
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