首页> 外文期刊>Biochemistry research international >Synthesis of Surfactants Derived from 2-Mercaptobenzimidazole and Study of Their Acute Toxicity and Analgesic and Psychotropic Activities
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Synthesis of Surfactants Derived from 2-Mercaptobenzimidazole and Study of Their Acute Toxicity and Analgesic and Psychotropic Activities

机译:衍生自2-巯基苯齐咪唑的表面活性剂的合成及其急性毒性和镇痛药和精神病药的研究

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The aim of the present study is to synthesize cationic salts from a relatively toxic compound named 2-mercaptobenzimidazole and to evaluate some of their pharmacological properties. The acute toxicity of these salts is evaluated according to OECD 423 Guidelines at the doses of 300 and 2000?mg/kg; their peripheral analgesic effect is studied using the Koster test at the therapeutic dose of 200?mg/kg and their sedative action is evaluated using Traction, Chimney, Hole-board, and Rotarod tests at the doses of 200 and 400?mg/kg. All synthesized molecules show no acute toxicity according to OECD Code 423 guidelines at doses ranging from 300 to 2000?mg/kg and do not cause any obesity or anorexia. Also, the results of the Koster test show that the studied compounds have an average analgesic effect at the dose of 200?mg/kg compared to acetylsalicylic acid. In addition, the elaborated compounds have shown a moderate sedative effect at the dose of 400?mg/kg, in comparison to 2-mercaptobenzimidazole (400?mg/kg) and Bromazepam (20?mg/kg). These compounds have no cataleptic and hypnotic effects on the central nervous system at the doses of 200 and 400?mg/kg. These results argue in favor of a possible integration of the most active salts tested in the pharmaceutical industry owing to their analgesic and sedative effects.
机译:本研究的目的是从一个名为2-巯基苯齐咪唑的相对有毒的化合物合成阳离子盐,并评估其一些药理学性质。这些盐的急性毒性根据经合组织423的剂量为300和2000〜2000毫克/千克的指南进行评价;使用200μmg/ kg治疗剂量的活性肌试验研究了它们的外周镇痛作用,并且使用牵引,烟囱,空穴板和旋转剂试验在200和400μg/ kg的剂量上进行评估它们的镇静作用。所有合成的分子都没有根据经合组织代码423的剂量的指南,从300〜2000?mg / kg的指南显示急性毒性,并且不会引起任何肥胖症或厌食症。此外,合作睾丸试验的结果表明,与乙酰胱氨酸相比,所研究的化合物的剂量为200μmmg/ kg的剂量为平均镇痛作用。此外,与2-巯基苯和kg)和Bromazepam(20×mg / kg)相比,所制定的化合物在400×mg / kg的剂量下显示了400×mg / kg的适度镇静效果。这些化合物在200和400μg/ kg的剂量下对中枢神经系统没有催化和催眠作用。这些结果有利于由于其镇痛和镇静作用而在制药行业中测试的最活跃的盐的可能集成。

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