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Synthesis, antimicrobial, and anti-inflammatory activity, of novel S-substituted and N-substituted 5-(1-adamantyl)-1,2,4-triazole-3-thiols

机译:新型S-取代和N-取代的5-(1-金刚烷基)-1,2,4-三唑-3-硫醇的合成,抗菌和抗炎活性

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Abstract: The reaction of 5-(1-adamantyl)-4-phenyl-1,2,4-triazoline-3-thione (compound 5) with formaldehyde and 1-substituted piperazines yielded the corresponding N-Mannich bases 6a–f. The reaction of 5-(1-adamantyl)-4-methyl-1,2,4-triazoline-3-thione 8 with various 2-aminoethyl chloride yielded separable mixtures of the S-(2-aminoethyl) 9a–d and the N-(2-aminoethyl) 10a–d derivatives. The reaction of compound 5 with 1-bromo-2-methoxyethane, various aryl methyl halides, and ethyl bromoacetate solely yielded the S-substituted products 11, 12a–d, and 13. The new compounds were tested for activity against a panel of Gram-positive and Gram-negative bacteria and the pathogenic fungus Candida albicans. Compounds 6b, 6c, 6d, 6e, 6f, 10b, 10c, 10d, 12c, 12d, 12e, 13, and 14 displayed potent antibacterial activity. Meanwhile, compounds 13 and 14 produced good dose-dependent anti-inflammatory activity against carrageenan-induced paw edema in rats.
机译:摘要:5-(1-金刚烷基)-4-苯基-1,2,4-三唑啉-3-硫酮(化合物5)与甲醛和1-取代的哌嗪的反应产生相应的N-曼尼希碱6a-f。 5-(1-金刚烷基)-4-甲基-1,2,4-三唑啉-3-硫酮8与各种2-氨基乙基氯化物的反应产生S-(2-氨基乙基)9a–d与苯甲酸酯的可分离混合物N-(2-氨基乙基)10a-d衍生物。化合物5与1-溴-2-甲氧基乙烷,各种芳基甲基卤化物和溴乙酸乙酯的反应仅产生S取代的产物11、12a–d和13。测试了新化合物对革兰氏化合物的活性。阳性和革兰氏阴性细菌以及致病真菌白色念珠菌。化合物6b,6c,6d,6e,6f,10b,10c,10d,12c,12d,12e,13和14显示出有效的抗菌活性。同时,化合物13和14对角叉菜胶诱导的爪水肿产生了良好的剂量依赖性抗炎活性。

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