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Kratko priopćenje

https://doi.org/10.2478/v10007-009-0026-7

Synthesis of some novel triazole derivatives as anti-nociceptive and anti-inflammatory agents

AIYALU RAJASEKARAN ; KMCH College of Pharmacy, Coimbatore, Tamilnadu, India
KALASALINGAM ANANDA RAJAGOPAL ; AK College of Pharmacy, Krishnankoil, Tamilnadu, India


Puni tekst: engleski pdf 82 Kb

str. 355-364

preuzimanja: 2.087

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Sažetak

Eight novel 1-[2-(1H-tetrazol-5-yl)ethyl]-1H-benzo[d][1,2,3]triazoles (3a-h) have been synthesized in order to obtain new compounds with potential anti-nociceptive and anti-inflammatory activity. The titled compounds were synthesized by the condensation of 1-[2-(1H-tetrazol-5-yl)ethyl]-1H-benzotriazole (2) and appropriate acid chlorides. Compound (2) was synthesized by reacting 3-(1H-benzo[d][1,2,3]triazol-1-yl)propanonitrile (1) with sodium azide and ammonium chloride in the presence of dimethylformamide. The synthesized compounds were characterized by spectroscopic methods (IR, 1H NMR, mass spectroscopy) and elemental analysis. The titled compounds were evaluated for anti-nociceptive activity by the hot plate method and the writhing response method and anti-inflammatory activity was evaluated by the carragenean induced paw edema method. 5-(2-(1H-benzo[d][1,2,3]triazo-1-yl)ethyl)-1H-tetrazol-1-yl)(4-aminophenyl)methanone (3d) and 5-(2-(1H-benzo[d][1,2,3]triazo-1-yl)ethyl)-1H-tetrazol-1-yl) (2-hydroxyphenyl)methanone (3g) exhibited significant anti-nociceptive activity. 1-(2-(1-Tosyl-1H-tetrazol-5-yl)ethyl)-1H-benzo[d][1,2,3]triazole (3c) and 4-5-(2-(1H-benzo[d][1,2,3]triazo-1-yl)ethyl)-1H-tetrazol-1-yl sulfonyl)benzenamine (3f) elicited superior anti-inflammatory activity compared to other synthesized compounds. Further investigations are needed to discern the mechanism of action.

Ključne riječi

synthesis; 1-[2-(1H-tetrazol-5-yl)ethyl]-1H-benzo[d][1,2,3]triazole; anti-nociception; inflammation

Hrčak ID:

38922

URI

https://hrcak.srce.hr/38922

Datum izdavanja:

1.9.2009.

Podaci na drugim jezicima: hrvatski

Posjeta: 3.445 *