7 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
Easily accessible polycyclic amines that inhibit the wild-type and amantadine-resistant mutants of the M2 channel of influenza A virus.
Universitat De Barcelona
Binding and Proton Blockage by Amantadine Variants of the Influenza M2
National and Kapodistrian University of Athens
Discovery of Highly Potent Inhibitors Targeting the Predominant Drug-Resistant S31N Mutant of the Influenza A Virus M2 Proton Channel.
The University of Arizona
Synthesis and structure-activity relationship study of arylsulfonamides as novel potent H5N1 inhibitors.
Wuhan University
Unraveling the Binding, Proton Blockage, and Inhibition of Influenza M2 WT and S31N by Rimantadine Variants.
National and Kapodistrian University of Athens
Quest for Novel Chemical Entities through Incorporation of Silicon in Drug Scaffolds.
Csir-National Chemical Laboratory