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A3- and A2B-fluorocorroles: synthesis, X-ray characterization and antiviral activity evaluation against human cytomegalovirus infection.
Kappler-Gratias, Sandrine; Bucher, Léo; Desbois, Nicolas; Rousselin, Yoann; Bystricky, Kerstin; Gros, Claude P; Gallardo, Franck.
Afiliação
  • Kappler-Gratias S; NeoVirTech , SAS , Institut des Technologies Avancées en sciences du Vivant (CNRS USR3505) , 1 place Pierre Potier, Oncopole , 31106 Toulouse , France . Email: fgallardo@neovirtech.com.
  • Bucher L; Institut de Chimie Moléculaire de l'Université de Bourgogne (ICMUB) , UMR CNRS 6302 , Université Bourgogne Franche-Comté , 9 Avenue Alain Savary, BP 47870 , 21078 Dijon Cedex , France . Email: Claude.Gros@u-bourgogne.fr.
  • Desbois N; Institut de Chimie Moléculaire de l'Université de Bourgogne (ICMUB) , UMR CNRS 6302 , Université Bourgogne Franche-Comté , 9 Avenue Alain Savary, BP 47870 , 21078 Dijon Cedex , France . Email: Claude.Gros@u-bourgogne.fr.
  • Rousselin Y; Institut de Chimie Moléculaire de l'Université de Bourgogne (ICMUB) , UMR CNRS 6302 , Université Bourgogne Franche-Comté , 9 Avenue Alain Savary, BP 47870 , 21078 Dijon Cedex , France . Email: Claude.Gros@u-bourgogne.fr.
  • Bystricky K; Centre de Biologie Intégrative (CBI) , Laboratoire de Biologie Moléculaire Eucaryote (LBME) , University of Toulouse , UPS , CNRS , Route de Narbonne , F-31062 Toulouse , France.
  • Gros CP; Institut Universitaire de France (IUF) , France.
  • Gallardo F; Institut de Chimie Moléculaire de l'Université de Bourgogne (ICMUB) , UMR CNRS 6302 , Université Bourgogne Franche-Comté , 9 Avenue Alain Savary, BP 47870 , 21078 Dijon Cedex , France . Email: Claude.Gros@u-bourgogne.fr.
RSC Med Chem ; 11(7): 783-801, 2020 Jul 01.
Article em En | MEDLINE | ID: mdl-33479675
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Med Chem Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Med Chem Ano de publicação: 2020 Tipo de documento: Article