首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Antimicrobial and Hypoglycemic Activities of Novel N-Mannich Bases Derived from 5-(1-Adamantyl)-4-substituted-124-triazoline-3-thiones
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Antimicrobial and Hypoglycemic Activities of Novel N-Mannich Bases Derived from 5-(1-Adamantyl)-4-substituted-124-triazoline-3-thiones

机译:5-(1-金刚烷基)-4-取代-124-三唑啉-3-硫酮衍生的新型N-曼尼希碱的抗微生物和降血糖活性

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摘要

The reaction of 5-(1-adamantyl)-4-ethyl or allyl-1,2,4-triazoline-3-thione with formaldehyde solution and various 1-substituted piperazines yielded the corresponding N-Mannich bases. The newly synthesized N-Mannich bases were tested for in vitro inhibitory activities against a panel of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Six compounds showed potent antibacterial activity against one or more of the tested microorganisms, while two compounds exhibited moderate activity against the tested Gram-positive bacteria. None of the newly synthesized compounds were proved to possess marked activity against Candida albicans. The oral hypoglycemic activity of six compounds was determined in streptozotocin (STZ)-induced diabetic rats. Four compounds produced significant strong dose-dependent reduction of serum glucose levels, compared to gliclazide at 10 mg/kg dose level (potency ratio > 75%).
机译:5-(1-金刚烷基)-4-乙基或烯丙基-1,2,4-三唑啉-3-硫酮与甲醛溶液和各种1-取代的哌嗪的反应产生相应的N-曼尼希碱。测试了新合成的N-曼尼希碱对一组革兰氏阳性和革兰氏阴性细菌以及酵母样病原真菌白色念珠菌的体外抑制活性。六种化合物对一种或多种被测微生物表现出有效的抗菌活性,而两种化合物对被测革兰氏阳性细菌表现出中等的活性。新合成的化合物均未证明对白色念珠菌具有显着活性。在链脲佐菌素(STZ)诱导的糖尿病大鼠中测定了六种化合物的口服降血糖活性。与10 mg / kg剂量的格列齐特相比,四种化合物产生显着的剂量依赖性强的血清葡萄糖水平降低(效价比> 75%)。

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