Department of Pharmacology, Faculty of Pharmacy, Anadolu University, 26470, Eskişehir, Turkey.
Arch Pharm Res. 2012 Mar;35(4):659-69. doi: 10.1007/s12272-012-0410-6. Epub 2012 May 3.
Novel thiadiazole derivatives bearing hydrazone moieties were synthesized through the reaction of 2-[(5-methyl-1,3,4-thiadiazol-2-yl)thio)]acetohydrazide with aldehydes/ketones. The chemical structures of the compounds were elucidated by (1)H-NMR, (13)C-NMR, MS-FAB spectral data, and elemental analyses. Behavioral effects of the test compounds in mice were examined by hole-board, activity cage, tail suspension and modified forced swimming tests (MFST). Antinociceptive activities were evaluated using the hot-plate and tail-clip methods. Results of the experiments indicated that the test compounds did not significantly change the exploratory behaviors or locomotor activities of animals in the hole-board and activity cage tests, respectively. Administration of the reference drug fluoxetine (10 mg/kg) and compounds 3a, 3b, 3c, 3j, 3k, and 3l significantly shortened the immobility times of animals in the tail suspension and MFST tests, indicating the antidepressant-like effects of these derivatives. Morphine (10 mg/kg) and compounds 3a, 3b, 3c, 3d, 3e, 3j, 3k, and 3l increased the reaction times of mice in both the hot-plate and tail-clip tests, indicating the antinociceptive effects of these compounds. To the best of our knowledge, this is the first study of central nervous system activities of chemical compounds carrying thiadiazole and hydrazone moieties together on their structures.
新型噻二唑衍生物通过 2-[(5-甲基-1,3,4-噻二唑-2-基)硫基]乙酰胺与醛/酮的反应合成。通过 (1)H-NMR、(13)C-NMR、MS-FAB 光谱数据和元素分析确定了化合物的化学结构。通过洞板、活动笼、悬尾和改良强迫游泳试验 (MFST) 检查了试验化合物在小鼠中的行为效应。使用热板和尾巴夹方法评估了镇痛活性。实验结果表明,试验化合物在洞板和活动笼试验中均未显著改变动物的探索行为或运动活性。参比药物氟西汀(10mg/kg)和化合物 3a、3b、3c、3j、3k 和 3l 的给药显著缩短了动物在悬尾和 MFST 试验中的不动时间,表明这些衍生物具有抗抑郁样作用。吗啡(10mg/kg)和化合物 3a、3b、3c、3d、3e、3j、3k 和 3l 增加了两种热板和尾巴夹试验中小鼠的反应时间,表明这些化合物具有镇痛作用。据我们所知,这是首次研究结构上同时带有噻二唑和腙基的化学化合物对中枢神经系统活性的研究。