Synthesis and antinociceptive activities of some pyrazoline derivatives

被引:95
|
作者
Kaplancikli, Zafer Asim [1 ]
Turan-Zitouni, Guelhan [1 ]
Ozdemir, Ahmet [1 ]
Can, Oezguer Devrim [2 ]
Chevallet, Pierre [3 ,4 ]
机构
[1] Anadolu Univ, Fac Pharm, Dept Pharmaceut Chem, TR-26470 Eskisehir, Turkey
[2] Anadolu Univ, Fac Pharm, Dept Pharmacol, TR-26470 Eskisehir, Turkey
[3] Univ Montpellier I, Inst Biomol Max Mousseron, UMR 5247, CNRS, Montpellier 5, France
[4] Univ Montpellier 2, Fac Pharm, Montpellier 5, France
关键词
Pyrazoline; Benzoxazole; Benzimidazole; Hot plate; Writhing test; Rota-Rod; NITRIC-OXIDE SYNTHASE; PHARMACOLOGICAL-PROPERTIES; ANTIINFLAMMATORY AGENTS; MICE; CYCLOOXYGENASE-2; INHIBITION; EXTRACT; POTENT; BASES; ACID;
D O I
10.1016/j.ejmech.2008.09.002
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In the present study, some pyrazoline derivatives were synthesized to investigate their potential antinociceptive activities. 1-[(Benzoxazole/benzimidazole-2-yl)thioacetyl]pyrazoline derivatives were obtained by reacting 3,5-diaryl-1-(2-chloroacetyl)pyrazolines with 2-marcaptobenzoxazole/benzimidazole. The chemical structures of the compounds were elucidated by IR, H-1 NMR and FAB(+)-MS spectral data and Elemental Analyses. All of the compounds (100 mg/kg) exhibited significant antinociceptive activities in both hot plate and acetic acid-induced writhing tests. Naloxone (5 mg/kg) pre-treatment reversed the antinociceptive activities suggesting the involvement of opioid system in the analgesic actions. None of the compounds impaired motor coordination of animals when assessed in the Rota-Rod model. These results support the previous papers reporting the opioid sensitive antinociceptive activities of various benzoxazole/benzimidazole-pyrazoline derivative compounds. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:2606 / 2610
页数:5
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