Literature DB >> 34197077

Medicinal Chemistry of Isocyanides.

Alberto Massarotti1, Francesca Brunelli1, Silvio Aprile1, Mariateresa Giustiniano2, Gian Cesare Tron1.   

Abstract

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.

Entities:  

Year:  2021        PMID: 34197077     DOI: 10.1021/acs.chemrev.1c00143

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  7 in total

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Authors:  Antonio Del Rio Flores; David W Kastner; Yongle Du; Maanasa Narayanamoorthy; Yuanbo Shen; Wenlong Cai; Vyshnavi Vennelakanti; Nicholas A Zill; Luisa B Dell; Rui Zhai; Heather J Kulik; Wenjun Zhang
Journal:  J Am Chem Soc       Date:  2022-03-07       Impact factor: 15.419

2.  Deciphering the Reaction Pathway of Mononuclear Iron Enzyme-Catalyzed N≡C Triple Bond Formation in Isocyanide Lipopeptide and Polyketide Biosynthesis.

Authors:  Tzu-Yu Chen; Ziyang Zheng; Xuan Zhang; Jinfeng Chen; Lide Cha; Yijie Tang; Yisong Guo; Jiahai Zhou; Binju Wang; Hung-Wen Liu; Wei-Chen Chang
Journal:  ACS Catal       Date:  2022-01-31       Impact factor: 13.700

3.  The Dark Side of Isocyanides: Visible-Light Photocatalytic Activity in the Oxidative Functionalization of C(sp3)-H Bonds.

Authors:  Camilla Russo; Jussara Amato; Gian Cesare Tron; Mariateresa Giustiniano
Journal:  J Org Chem       Date:  2021-12-01       Impact factor: 4.354

4.  Hydroarylation of enamides enabled by HFIP via a hexafluoroisopropyl ether as iminium reservoir.

Authors:  Nicolas Zeidan; Sergiu Bicic; Robert J Mayer; David Lebœuf; Joseph Moran
Journal:  Chem Sci       Date:  2022-06-27       Impact factor: 9.969

5.  Anti-inflammatory aromadendrane- and cadinane-type sesquiterpenoids from the South China Sea sponge Acanthella cavernosa.

Authors:  Shou-Mao Shen; Qing Yang; Yi Zang; Jia Li; Xueting Liu; Yue-Wei Guo
Journal:  Beilstein J Org Chem       Date:  2022-07-25       Impact factor: 2.544

6.  N-Formylsaccharin: A Sweet(able) Formylating Agent in Mechanochemistry.

Authors:  Federico Cuccu; Francesco Basoccu; Claudia Fattuoni; Andrea Porcheddu
Journal:  Molecules       Date:  2022-08-25       Impact factor: 4.927

7.  Experimental Treatment of Hazardous Ash Waste by Microbial Consortium Aspergillus niger and Chlorella sp.: Decrease of the Ni Content and Identification of Adsorption Sites by Fourier-Transform Infrared Spectroscopy.

Authors:  Alexandra Šimonovičová; Alžbeta Takáčová; Ivan Šimkovic; Sanja Nosalj
Journal:  Front Microbiol       Date:  2021-12-07       Impact factor: 5.640

  7 in total

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