Paper Report for: Wieckowska_2010_Eur.J.Med.Chem_45_5602
Reference
Title: Novel alkyl- and arylcarbamate derivatives with N-benzylpiperidine and N-benzylpiperazine moieties as cholinesterases inhibitors Wieckowska A, Bajda M, Guzior N, Malawska B Ref: Eur Journal of Medicinal Chemistry, 45:5602, 2010 : PubMed
The study presents synthesis and biological activity of novel alkyl- and arylcarbamate derivatives with N-benzylpiperidine and N-benzylpiperazine moieties designed as cholinesterases inhibitors. These fragments turned out to determine compounds' selectivity between AChE and BuChE. Derivatives of N-benzylpiperazine (16-25) were selective BuChE inhibitors with 3-(2-(4-benzylpiperazin-1-yl)-2-oxoethyl)-phenyl butylcarbamate (22) being the most potent compound (pIC50=5.00) while a series of carbamate derivatives of N-benzylpiperidine (5-14) displayed non-selective BuChE/AChE inhibitory activity. Molecular modelling studies point out significant differences between orientations of these two groups of compounds in the active site of AChE, which can be an explanation of their different biological activity.
        
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Wieckowska A, Bajda M, Guzior N, Malawska B (2010) Novel alkyl- and arylcarbamate derivatives with N-benzylpiperidine and N-benzylpiperazine moieties as cholinesterases inhibitors Eur Journal of Medicinal Chemistry45: 5602-11
Wieckowska A, Bajda M, Guzior N, Malawska B (2010) Eur Journal of Medicinal Chemistry45: 5602-11