Xanthates and Trithiocarbonates Strongly Inhibit Carbonic Anhydrases and Show Antiglaucoma Effects in Vivo

被引:83
作者
Carta, Fabrizio [1 ]
Akdemir, Atilla [2 ]
Scozzafava, Andrea [1 ]
Masini, Emanuela [3 ]
Supuran, Claudiu T. [1 ,4 ]
机构
[1] Univ Florence, Lab Chim Bioinorgan, I-50019 Florence, Italy
[2] Bezmialem Vakif Univ, Dept Pharmacol, Fac Pharm, TR-34093 Istanbul, Turkey
[3] Univ Florence, Preclin & Clin Pharmacol Sect, NEUROFARBA Dept, I-50139 Florence, Italy
[4] Univ Florence, Sez Sci Farmaceut & Nutraceut, NEUROFARBA Dept, I-50019 Florence, Italy
关键词
ISOFORMS-I; ACTIVATORS; COUMARINS; MECHANISM; PHENOLS; VII; XIV;
D O I
10.1021/jm400414j
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Dithiocarbamates (DTCs) were recently discovered as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors. A series of xanthates and a trithiocarbonate, structurally related to the DTCs, were prepared by reaction of alcohols/thiols with carbon disulfide in the presence of bases. These compounds were tested for the inhibition of four human (h) isoforms, hCA I, II, a, and XII, involved in pathologies such as glaucoma (CA II and XII) or cancer (CA IX). Several low nanomolar xanthate/trithiocarbonate inhibitors targeting these CM were detected. A docking study of some xanthates within the CA II active site showed that these compounds bind in a similar manner with the dithiocarbamates, coordinating monodentately to the Zn(II) ion from the enzyme active site. Several xanthates showed potent intraocular pressure lowering activity in two animal models of glaucoma via the topical administration. Xanthates and thioxanthates represent two novel, promising classes of CA inhibitors.
引用
收藏
页码:4691 / 4700
页数:10
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