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Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping.
Authors:W J Brouillette  V R Atigadda  M Luo  G M Air  Y S Babu  S Bantia
Affiliation:Department of Chemistry, University of Alabama at Birmingham, 35294, USA.
Abstract:A 2-pyrrolidinone ring containing a single hydroxymethyl side chain effectively replaces the N-acetylamino group of 4-(N-acetylamino)-3-guanidinobenzoic acid, a low micromolar inhibitor of influenza neuraminidase. This novel structural template affords new opportunities to evolve more potent benzoic acid inhibitors.
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