Design, Synthesis, Binding, Crystallography, and Docking of [(2-Pyrimidinylthio)Acetyl]Benzenesulfonamides as Inhibitors of Human Carbonic Anhydrases

Biophysical Journal- United States

doi 10.1016/j.bpj.2012.11.3095

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January 1, 2013

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Elsevier BV

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Design, Synthesis, Binding, Crystallography, and Docking of [(2-Pyrimidinylthio)Acetyl]Benzenesulfonamides as Inhibitors of Human Carbonic Anhydrases

Biophysical Journal- United States

Full Text

Abstract

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Date

Authors

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4-Amino-Substituted Benzenesulfonamides as Inhibitors of Human Carbonic Anhydrases

Intrinsic Thermodynamics and Structure Correlation of Benzenesulfonamides With a Pyrimidine Moiety Binding to Carbonic Anhydrases I, II, VII, XII, and XIII

Synthesis, Spectral Characterization, Docking Studies and QSAR Screening of 4-Amino-Benzenesulfonamides/N-Acetyl 4-Amino-Benzenesulfonamide Derivatives as Antimicrobial Agents

Appraisal of Anti-Protozoan Activity of Nitroaromatic Benzenesulfonamides Inhibiting Carbonic Anhydrases From Trypanosoma Cruzi and Leishmania Donovani

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