首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, antimicrobial and anti-inflammatory activities of novel 5-(1-adamantyl)-1,3,4-thiadiazole derivatives.
【24h】

Synthesis, antimicrobial and anti-inflammatory activities of novel 5-(1-adamantyl)-1,3,4-thiadiazole derivatives.

机译:新型5-(1-氨烷基)-1,3,4-噻二唑衍生物的合成,抗微生物和抗炎活性。

获取原文
获取原文并翻译 | 示例
           

摘要

New 1-adamanyl-1,3,4-thiadiazole derivatives namely, 5-(1-adamantyl)-1,3,4-thiadiazoline-2-thione 3, 5-(1-adamantyl)-3-(benzyl- or 4-substituted benzyl)-1,3,4-thiadiazoline-2-thione 4a-d, 5-(1-adamantyl)-3-(4-substituted-1-piperazinylmethyl)-1,3,4-thiadiazoline-2-thion es 5a-c, 2-[5-(1-adamantyl)-2-thioxo-1,3,4-thiadiazolin-3-yl]acetic acid 7, (+/-)-2-[5-(1-adamantyl)-2-thioxo-1,3,4-thiadiazolin-3-yl]propionic acid 9, 3-[5-(1-adamantyl)-2-thioxo-1,3,4-thiadiazolin-3-yl]propionic acid 11, N-[5-(1-adamantyl)-1,3,4-thiadiazol-2-yl]-N'-arylthioureas 15a-c and 5-(1-adamantyl)-1,3,4-thiadiazoline-2-one 16, were synthesized and tested for in vitro activities against a panel of gram-positive and gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Compounds 7, 9, 15b and 15c displayed marked activity against the tested gram-positive bacteria, while compound 3 was highly active against the tested gram-negative bacteria. Compounds 4b, 7 and 15c were weakly or moderately active against C. albicans. In addition, the in vivo anti-inflammatory activity of the synthesized compounds was determined using the carrageenan-induced paw oedema method in rats. The propionic acid derivative 9 produced good dose-dependent anti-inflammatory activity.
机译:新的1-咪唑-1,3,4-噻二唑衍生物即,5-(1-亚氨基烷基)-1,3,4-噻二唑啉-2-尖头3,5-(1-亚氨基烷基)-3-(苄基或4-取代的苄基)-1,3,4-噻唑啉-2-倍六酮4a-d,5-(1-亚氨基烷基)-3-(4-取代-1-哌嗪基甲基)-1,3,4-噻二唑啉-2 - es es 5a-c,2- [5-(1-亚氨烷基)-2-硫代-1,3,4-噻二唑啉-3-基]乙酸7,(+/-) - 2- [5-( 1-亚氨基烷基)-2-硫代氧基-1,3,4-噻二唑啉-3-基]丙酸9,3- [5-(1-亚氨基烷基)-2-硫代吡啶-3-丙酸11,N- [5-(1-氨烷基)-1,3,4-噻二唑-2-基] -N'-芳基硫脲15a-c和5-(1-亚氨基烷基)-1,3, 4-噻二唑啉-2-116,用于对革兰氏阳性和革兰氏阴性细菌和酵母状病原菌念珠菌念珠菌的体外活性进行合成和测试。化合物7,9,5b和15c针对测试的革兰氏阳性细菌显示出显着的活性,而化合物3对测试的革兰氏阴性细菌具有高度活性。化合物4b,7和15c对C. albicans无弱或中度活性。此外,使用卡拉胶诱导的大鼠诱导的爪子水肿方法测定合成化合物的体内抗炎活性。丙酸衍生物9产生良好的剂量依赖性抗炎活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号