Orally Active Fusion Inhibitor of Respiratory Syncytial Virus

Author:

Cianci Christopher1,Yu Kuo-Long1,Combrink Keith1,Sin Ny1,Pearce Bradley1,Wang Alan1,Civiello Rita1,Voss Stacey1,Luo Guangxiang1,Kadow Kathy1,Genovesi Eugene V.1,Venables Brian1,Gulgeze Hatice1,Trehan Ashok1,James Jennifer1,Lamb Lucinda1,Medina Ivette1,Roach Julia1,Yang Zheng1,Zadjura Lisa1,Colonno Richard1,Clark Junius1,Meanwell Nicholas1,Krystal Mark1

Affiliation:

1. The Bristol-Myers Squibb Pharmaceutical Research Institute, Wallingford, Connecticut 06492

Abstract

ABSTRACT BMS-433771 was found to be a potent inhibitor of respiratory syncytial virus (RSV) replication in vitro. It exhibited excellent potency against multiple laboratory and clinical isolates of both group A and B viruses, with an average 50% effective concentration of 20 nM. Mechanism-of-action studies demonstrated that BMS-433771 inhibits the fusion of lipid membranes during both the early virus entry stage and late-stage syncytium formation. After isolation of resistant viruses, resistance was mapped to a series of single amino acid mutations in the F1 subunit of the fusion protein. Upon oral administration, BMS-433771 was able to reduce viral titers in the lungs of mice infected with RSV. This new class of orally active RSV fusion inhibitors offers potential for clinical development.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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