Chiral separation of new sulfonamide derivatives and evaluation of their enantioselective affinity for human carbonic anhydrase II by microscale thermophoresis and surface plasmon resonance

Author:

Rogez-Florent Tiphaine,Foulon Catherine,Drucbert Anne-Sophie,Schifano Nadège,Six Perrine,Devassine Stéphanie,Depreux Patrick,Danzé Pierre-Marie,Goossens Laurence,Danel Cécile,Goossens Jean-François

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference29 articles.

1. Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors;De Simone;Expert Opin. Drug Discov.,2013

2. Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms?;Alterio;Chem. Rev.,2012

3. Carbonic anhydrase inhibitors: an editorial;Supuran;Expert Opin. Ther. Pat.,2013

4. The carbon dioxide hydration activity of carbonic anhydrase. I. Stop-flow kinetic studies on the native human isoenzymes B and C;Khalifah;J. Biol. Chem.,1971

5. Insights towards sulfonamide drug specificity in α-carbonic anhydrases;Aggarwal;Bioorg. Med. Chem.,2013

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