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Turkish Journal of Chemistry

DOI

10.3906/kim-1612-76

Abstract

In this study, a series of benzimidazole-piperidine derivatives were synthesized with the objective of developing potent antinociceptive agents. Some 2-(4-substituted-phenyl)-1-[2-(piperidin-1-yl)ethyl]-1$H$-benzimidazole derivatives were obtained by microwave-supported reaction of an appropriate 2-(4-substituted-phenyl)-1$H$-benzimidazole with 2-(piperidine-1-yl)ethyl chloride. The chemical structures of the compounds were elucidated by FT-IR, $^{1}$H NMR, $^{13}$C NMR, and HRMS spectral data. Antinociceptive activity was assessed by conducting hot-plate, paw-pressure, and formalin tests. Morphine (5 mg/kg, i.p) was used as a reference drug. Among the tested compounds 2a-2d and 2f-2h (10 mg/kg) increased the maximum possible effect (MPE) % values calculated for the hot-plate and paw-pressure tests and decreased the paw licking time of rats in the early phase of the formalin test, indicating centrally mediated antinociceptive activities of these derivatives. In the late-phase 2g and 2h were the only compounds reducing the paw licking duration. These data show additional peripherally mediated antinociceptive activities for these two derivatives. Falling latencies of animals in the rotarod test did not change upon the administration of test compounds; thus, the observed antinociceptive effects were specific. Predictions obtained by theoretical calculations of ADME (absorption, distribution, metabolism, excretion) properties supported the antinociceptive potential of the tested benzimidazole-piperidine derivatives.

Keywords

Benzimidazole, formalin test, hot-plate test, paw-pressure test, piperidine, rotarod

First Page

672

Last Page

684

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