Discovery of highly potent agents against influenza A virus

Discovery of highly potent agents against influenza A virus Identification of camphor derivatives as novel M2 ion channel inhibitors of influenza A virus Imidazole-based pinanamine derivatives: Discovery of dual inhibitors of the wild-type and drug-resistant mutant of the influenza A virus Novel spirothiazamenthane inhibitors of the influenza A M2 proton channel Identification of Hits as Matrix-2 Protein Inhibitors through the Focused Screening of a Small Primary Amine Library 3-Azatetracyclo[5.2.1.1^5,8.0^1,5]undecane Derivatives: From Wild-Type Inhibitors of the M2 Ion Channel of Influenza A Virus to Derivatives with Potent Activity against the V27A Mutant Easily Accessible Polycyclic Amines that Inhibit the Wild-Type and Amantadine-Resistant Mutants of the M2 Channel of Influenza A Virus Discovery of Novel Dual Inhibitors of the Wild-Type and the Most Prevalent Drug-Resistant Mutant, S31N, of the M2 Proton Channel from Influenza A Virus Discovery of Highly Potent Inhibitors Targeting the Predominant Drug-Resistant S31N Mutant of the Influenza A Virus M2 Proton Channel Synthesis and Antiviral Activity Evaluation of Some New Aminoadamantane Derivatives. 2