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首页> 外文期刊>Research Letters in Biochemistry >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&2000  mg / kg的剂量评估了这些盐的急性毒性。通过在200&#X2009的治疗剂量的疗效剂量下使用活性肌试验研究了它们的外周镇痛作用。使用牵引,烟囱,空穴板和200和400&#x2009的剂量评估它们的镇静作用。 mg / kg。所有合成的分子都没有根据经合组织代码423的剂量的指南显示急性毒性范围从300至2000  mg / kg,并且不会引起任何肥胖症或厌食症。此外,活性肌试验结果表明,与乙酰山酸相比,所研究的化合物具有200  mg / kg的剂量的平均镇痛作用。此外,阐述的化合物在400  mg / kg的剂量下显示了适度的镇静效果,与2-巯基苯咪唑(400  mg / kg)和bromazepam(20  mg / kg)相比。这些化合物在200和400℃的中枢神经系统上对中枢神经系统没有催化和催眠作用; Mg / kg。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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