Name | 1-cyclopropyl-3-[[1-(4-hydroxybutyl)benzimidazol-2-yl]methyl]imidazo[4,5-c]pyridin-2-one |
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Synonyms | BMS433771 |
Description | BMS-433771 is a potent orally active inhibitor of respiratory syncytial virus (RSV). BMS-433771 is active against both A and B groups of RSV, with an average EC50 of 20 nM. BMS-433771 can be used for the research of respiratory tract disease[1][2]. |
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Related Catalog | |
Target |
EC50: 20 nM (RSV)[1] |
In Vitro | BMS-433771 has inhibitory against both A and B groups of RSV, with an average EC50 of 20 nM[1]. BMS-433771 can inhibit viral F protein-induced membrane fusion[1]. |
In Vivo | BMS-433771 (p.o.; 1-200 mg/kg; single or bid 4 days) shows prophylactic efficacy via oral dosing,but has considerable pharmacodynamic differences between the two rodent models[2] . Animal Model: rodent models of RSV infection[2] (cotton rat and mice) Dosage: 1, 10, and 50 mg/kg (mice); 25, 50, 100, and 200 mg/kg (rat) Administration: oral, single or bid 4 days Result: Had prophylactic efficacy via oral dosing in both animal models. Showed RSV infection more sensitive to inhibition in the BALB/c mouse host than in the cotton rat. |
Molecular Formula | C21H23N5O2 |
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Molecular Weight | 377.44000 |
Exact Mass | 377.18500 |
PSA | 77.87000 |
LogP | 2.70340 |