Phosphorus versus Sulfur: Discovery of Benzenephosphonamidates as Versatile Sulfonamide-Mimic Chemotypes Acting as Carbonic Anhydrase Inhibitors

被引:47
作者
Nocentini, Alessio [1 ,2 ]
Gratteri, Paola [1 ]
Supuran, Claudiu T. [2 ]
机构
[1] Univ Firenze, Dept NEUROFARBA, Pharmaceut & Nutraceut Sect, Lab Mol Modeling Cheminformat & QSAR, Via Ugo Schiff 6, I-50019 Sesto Fiorentino, Italy
[2] Univ Firenze, Dept NEUROFARBA, Pharmaceut & Nutraceut Sect, Via Ugo Schiff 6, I-50019 Sesto Fiorentino, Italy
关键词
carbonic anhydrase; inhibition; metallo-enzymes; MM-GBSA; phosphonamidate; QPLD; zinc-binder; ZINC-BINDING GROUP; PHOSPHONAMIDATE; IX;
D O I
10.1002/chem.201805039
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The first zinc-binding group (ZBG) to have been identified as inhibitor of the metallo-enzymes carbonic anhydrases (CA, EC 4.2.1.1) was the sulfonamide. From then on several classes of zinc-binders have been described. This work reports the benzenephosponamidates as a new chiral aromatic sulfonamide-mimic ZBG able to meet the requirements for effectively binding the enzyme active site. Several low micromolar CA I, II, VII, IX inhibitors were thus detected. Kinetic studies, QM-polarized ligand docking, and MM-GBSA in silico methods were used to characterize this newly identified CA inhibitor chemotype.
引用
收藏
页码:1188 / 1192
页数:5
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