Cianci Christopher, Yu Kuo-Long, Combrink Keith, Sin Ny, Pearce Bradley, Wang Alan, Civiello Rita, Voss Stacey, Luo Guangxiang, Kadow Kathy, Genovesi Eugene V, Venables Brian, Gulgeze Hatice, Trehan Ashok, James Jennifer, Lamb Lucinda, Medina Ivette, Roach Julia, Yang Zheng, Zadjura Lisa, Colonno Richard, Clark Junius, Meanwell Nicholas, Krystal Mark
The Bristol-Myers Squibb Pharmaceutical Research Institute, Wallingford, Connecticut 06492, USA.
Antimicrob Agents Chemother. 2004 Feb;48(2):413-22. doi: 10.1128/AAC.48.2.413-422.2004.
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.
发现BMS-433771在体外是呼吸道合胞病毒(RSV)复制的强效抑制剂。它对A组和B组病毒的多种实验室和临床分离株均表现出优异的效力,平均50%有效浓度为20 nM。作用机制研究表明,BMS-433771在病毒早期进入阶段和晚期合胞体形成过程中均抑制脂质膜融合。分离出耐药病毒后,耐药性定位到融合蛋白F1亚基中的一系列单氨基酸突变。口服给药后,BMS-433771能够降低感染RSV的小鼠肺部的病毒滴度。这类新型口服活性RSV融合抑制剂具有临床开发潜力。