| Literature DB >> 29220568 |
Rosana Leiva1, Marta Barniol-Xicota1, Sandra Codony1, Tiziana Ginex2, Evelien Vanderlinden3, Marta Montes1, Michael Caffrey4, F Javier Luque2, Lieve Naesens3, Santiago Vázquez1.
Abstract
Two series of easily accessible anilines were identified as inhibitors of influenza A virus subtype H1N1, and extensive chemical synthesis and analysis of the structure-activity relationship were performed. The compounds were shown to interfere with low pH-induced membrane fusion mediated by the H1 and H5 (group 1) hemagglutinin (HA) subtypes. A combination of virus resistance, HA interaction, and molecular dynamics simulation studies elucidated the binding site of these aniline-based influenza fusion inhibitors, which significantly overlaps with the pocket occupied by some H3 HA-specific inhibitors, indicating the high relevance of this cavity for drug design.Entities:
Mesh:
Substances:
Year: 2017 PMID: 29220568 DOI: 10.1021/acs.jmedchem.7b00908
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446