| Literature DB >> 29341607 |
Yuanxiang Wang1, Yanmei Hu1, Shuting Xu1, Yongtao Zhang1, Rami Musharrafieh2, Raymond Kin Hau1, Chunlong Ma3, Jun Wang1,3.
Abstract
Influenza viruses are respiratory pathogens that are responsible for both seasonal influenza epidemics and occasional influenza pandemics. The narrow therapeutic window of oseltamivir, coupled with the emergence of drug resistance, calls for the next-generation of antivirals. With our continuous interest in developing AM2-S31N inhibitors as oral influenza antivirals, we report here the progress of optimizing the in vitro pharmacokinetic (PK) properties of AM2-S31N inhibitors. Several AM2-S31N inhibitors, including compound 10b, were discovered to have potent channel blockage, single to submicromolar antiviral activity, and favorable in vitro PK properties. The antiviral efficacy of compound 10b was also synergistic with oseltamivir carboxylate. Interestingly, binding kinetic studies (Kd, Kon, and Koff) revealed several AM2-S31N inhibitors that have similar Kd values but significantly different Kon and Koff values. Overall, this study identified a potent lead compound (10b) with improved in vitro PK properties that is suitable for the in vivo mouse model studies.Entities:
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Year: 2018 PMID: 29341607 PMCID: PMC6445276 DOI: 10.1021/acs.jmedchem.7b01536
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446