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新型2-[3-(1-金刚烷基)-4-取代-5-硫代-1,2,4-三唑啉-1-基]乙酸、2-[3-(1-金刚烷基)-4-取代-5-硫代-1,2,4-三唑啉-1-基]丙酸及相关衍生物的合成、抗菌和抗炎活性

Synthesis, antimicrobial, and anti-inflammatory activities of novel 2-[3-(1-adamantyl)-4-substituted-5-thioxo-1,2,4-triazolin-1-yl] acetic acids, 2-[3-(1-adamantyl)-4-substituted-5-thioxo-1,2,4-triazolin-1-yl]propionic acids and related derivatives.

作者信息

Al-Deeb Omar A, Al-Omar Mohamed A, El-Brollosy Nasser R, Habib Elsayed E, Ibrahim Tarek M, El-Emam Ali A

机构信息

Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

出版信息

Arzneimittelforschung. 2006;56(1):40-7. doi: 10.1055/s-0031-1296699.

Abstract

The reaction of 3-(1-adamantyl)-4-substituted-1,2,4-triazoline-5-thiones 3a-g with sodium chloroacetate, in ethanolic sodium hydroxide yielded the corresponding N1-acetic acid derivatives 4a-g. The interaction of 3a-g with ethyl 2-bromopropionate in acetone, in the presence of potassium carbonate, yielded the corresponding N1-ethyl propionate derivatives 5a-g, which upon hydrolysis with aqueous sodium hydroxide afforded the corresponding propionic acid derivatives 6a-g. Similarly, the reaction of 3-(1-adamantyl)-4-amino-1,2,4-triazoline-5-thione 7 with sodium chloroacetate in ethanolic sodium hydroxide yielded the corresponding N1-acetic acid derivative 8. On the other hand, the reaction of 2-(1-adamantyl)-1,3,4-oxadiazoline-5-thione 9 with sodium chloroacetate yielded the corresponding S-acetic acid derivative 10. Compounds 4a-g, 5b, 5c, 5g, 6a-g, 8 and 10 were tested for in vitro activities against a panel of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Several derivatives produced good or moderate activities particularly against Bacillus subtilis. In addition, the in vivo anti-inflammatory activities of these compounds were determined using the carrageenin-induced paw oedema method in rats. Compounds 4a, 4b, 4e, 4f, 6f, 6g and 10 produced good dose-dependent anti-inflammatory activities.

摘要

3-(1-金刚烷基)-4-取代-1,2,4-三唑啉-5-硫酮3a-g与氯乙酸钠在乙醇钠氢氧化物中反应,生成相应的N1-乙酸衍生物4a-g。3a-g与2-溴丙酸乙酯在丙酮中、碳酸钾存在下反应,生成相应的N1-丙酸乙酯衍生物5a-g,5a-g用氢氧化钠水溶液水解得到相应的丙酸衍生物6a-g。类似地,3-(1-金刚烷基)-4-氨基-1,2,4-三唑啉-5-硫酮7与氯乙酸钠在乙醇钠氢氧化物中反应,生成相应的N1-乙酸衍生物8。另一方面,2-(1-金刚烷基)-1,3,4-恶二唑啉-5-硫酮9与氯乙酸钠反应,生成相应的S-乙酸衍生物10。对化合物4a-g、5b、5c、5g、6a-g、8和10进行了针对一组革兰氏阳性和革兰氏阴性细菌以及酵母样致病真菌白色念珠菌的体外活性测试。几种衍生物产生了良好或中等的活性,特别是对枯草芽孢杆菌。此外,使用角叉菜胶诱导的大鼠足爪水肿法测定了这些化合物的体内抗炎活性。化合物4a、4b、4e、4f、6f、6g和10产生了良好的剂量依赖性抗炎活性。

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