Synthesis and structure-activity relationships of novel benzene sulfonamides with potent binding affinity for bovine carbonic anhydrase II

Bioorg Med Chem Lett. 2005 Dec 15;15(24):5429-33. doi: 10.1016/j.bmcl.2005.08.113. Epub 2005 Oct 6.

Abstract

This manuscript reports the identification of a novel series of mono- and bis- benzene sulfonamides with potent binding affinity for bovine carbonic anhydrase II (bCAII). These compounds exhibited nanomolar equilibrium dissociation constants with K(i)'s ranging from 4.7 to 9.3nM. All compounds were ester derivatives of the weak affinity bCAII inhibitor, 4-carboxybenzenesulfonamide. Structure-activity relationships for this novel series of compounds are discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzene Derivatives / chemical synthesis
  • Benzene Derivatives / pharmacokinetics*
  • Binding Sites
  • Carbonic Anhydrase II / metabolism*
  • Cattle
  • Crystallography, X-Ray
  • Models, Molecular
  • Molecular Conformation
  • Sulfonamides / chemical synthesis
  • Sulfonamides / pharmacokinetics*

Substances

  • Benzene Derivatives
  • Sulfonamides
  • Carbonic Anhydrase II