Alterio Vincenzo, Esposito Davide, Monti Simona Maria, Supuran Claudiu T, De Simone Giuseppina
a Istituto di Biostrutture e Bioimagini-CNR , Naples , Italy.
b Neurofarba Department, Section of Pharmaceutical and Nutraceutical Sciences , Università degli Studi di Firenze , Sesto Fiorentino, Florence , Italy.
J Enzyme Inhib Med Chem. 2018 Dec;33(1):151-157. doi: 10.1080/14756366.2017.1405263.
Pyridinium containing sulfonamides have been largely investigated as carbonic anhydrase inhibitors (CAIs), showing interesting selectivity features. Nevertheless, only few structural studies are so far available on adducts that these compounds form with diverse CA isoforms. In this paper, we report the structural characterization of the adduct that a triphenylpyridinium derivative forms with hCA II, showing that the substitution of the pyridinium ring plays a key role in determining the conformation of the inhibitor in the active site and consequently the binding affinity to the enzyme. These findings open new perspectives on the basic structural requirements for designing sulfonamide CAIs with a selective inhibition profile.
含吡啶鎓的磺胺类化合物作为碳酸酐酶抑制剂(CAIs)已得到大量研究,显示出有趣的选择性特征。然而,迄今为止,关于这些化合物与不同CA同工型形成的加合物的结构研究还很少。在本文中,我们报道了一种三苯基吡啶鎓衍生物与hCA II形成的加合物的结构表征,表明吡啶鎓环的取代在决定抑制剂在活性位点的构象以及因此对酶的结合亲和力方面起着关键作用。这些发现为设计具有选择性抑制谱的磺胺类CAIs的基本结构要求开辟了新的前景。