| Literature DB >> 33479675 |
Sandrine Kappler-Gratias1, Léo Bucher2, Nicolas Desbois2, Yoann Rousselin2, Kerstin Bystricky3,4, Claude P Gros2, Franck Gallardo1.
Abstract
Twenty-nine fluorinated corroles were prepared, spectroscopically characterized, and studied for their antiviral activity against human cytomegalovirus infection. Six corroles were also fully characterized by X-ray crystallography giving insights on their geometrical features. The halogenated corroles reported herein exhibit significantly improved antiviral activity over their non-halogenated counterparts and over nitro-corrole analogs previously reported. Full activity of thirteen A3-corroles is achieved with four fluorine atoms present on the meso-phenyl ring reaching a selectivity index above 300. The maximum activity is achieved for A2B-corroles with selectivity indexes above 400. We thus demonstrate that the fluorocorrole is a highly potent platform to synthesize a new generation of anti hCMV molecules. This journal is © The Royal Society of Chemistry 2020.Entities:
Year: 2020 PMID: 33479675 PMCID: PMC7496305 DOI: 10.1039/d0md00127a
Source DB: PubMed Journal: RSC Med Chem ISSN: 2632-8682