| Literature DB >> 28057408 |
Daniela Vullo1, Sonia Del Prete2, Alessio Nocentini3, Sameh M Osman4, Zeid AlOthman4, Clemente Capasso5, Murat Bozdag1, Fabrizio Carta3, Paola Gratteri6, Claudiu T Supuran7.
Abstract
A series of dithiocarbamates (DTCs) was investigated for the inhibition of the β-class carbonic anhydrase (CAs, EC 4.2.1.1) from the fungal parasite Malassezia globosa, MgCA, a validated anti-dandruff drug target. These DTCs incorporate various scaffold, among which those of N,N-dimethylaminoethylenediamine, the aminoalcohols with 3-5 carbon atoms in their molecule, 3-amino-quinuclidine, piperidine, morpholine and piperazine derivatives, as well as phenethylamine and its 4-sulfamoylated derivative. Several DTCs resulted more effective in inhibiting MgCA compared to the standard sulfonamide drug acetazolamide (KI of 74μM), with KIs ranging between 383 and 6235nM. A computational approach, involving a homology modeling of the enzyme and docking inhibitors within its active site, helped us rationalize the results. This study may contribute to better understand the inhibition profile of MgCA, and offer new ideas for the design of modulators of activity which belong to less investigated chemical classes, thus potentially useful to combat dandruff and other fungal infections.Entities:
Keywords: Carbonic anhydrase; Dithiocarbamate; Inhibitor; Malassezia globosa; β-CA-class enzyme
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Year: 2016 PMID: 28057408 DOI: 10.1016/j.bmc.2016.12.040
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641