Orally Active Fusion Inhibitor of Respiratory Syncytial Virus

Christopher Cianci(Bristol-Myers Squibb (United States)), Kuo‐Long Yu(Bristol-Myers Squibb (United States)), Keith D. Combrink(Bristol-Myers Squibb (United States)), Ny Sin(Bristol-Myers Squibb (United States)), Bradley C. Pearce(Bristol-Myers Squibb (United States)), Alan Wang(Bristol-Myers Squibb (United States)), Rita L. Civiello(Bristol-Myers Squibb (United States)), Stacey Voss(Bristol-Myers Squibb (United States)), Guangxiang Luo(Bristol-Myers Squibb (United States)), Kathy Kadow(Bristol-Myers Squibb (United States)), Eugene V. Genovesi(Bristol-Myers Squibb (United States)), Brian L. Venables(Bristol-Myers Squibb (United States)), H. Belgin Gülgeze(Bristol-Myers Squibb (United States)), Ashok K. Trehan(Bristol-Myers Squibb (United States)), Jennifer James(Bristol-Myers Squibb (United States)), Lucinda Lamb(Bristol-Myers Squibb (United States)), Ivette Medina(Bristol-Myers Squibb (United States)), Julia Roach(Bristol-Myers Squibb (United States)), Zheng Yang(Bristol-Myers Squibb (United States)), Lisa Zadjura(Bristol-Myers Squibb (United States)), Richard J. Colonno(Bristol-Myers Squibb (United States)), Junius M. Clark(Bristol-Myers Squibb (United States)), Nicholas A. Meanwell(Bristol-Myers Squibb (United States)), Mark Krystal(Bristol-Myers Squibb (United States))
Antimicrobial Agents and Chemotherapy
January 24, 2004
Cited by 139Open Access
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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.


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