...
首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis and Biological Evaluation of Naphthopyranopyrimidines Derivatives as Potential Antifungal and Antibacterial Activities
【24h】

Synthesis and Biological Evaluation of Naphthopyranopyrimidines Derivatives as Potential Antifungal and Antibacterial Activities

机译:萘吡喃并嘧啶类衍生物的合成和生物评价作为潜在的抗真菌和抗菌活性

获取原文
获取原文并翻译 | 示例
           

摘要

A new series of novel 8,10-dimethyl-12-aryl-12H-naphtho[1',2,5,6]pyrano[2,3-d]pyrimidine-9,11-diones derivatives synthesized from coupling (3CC) of aldehydes, β-naphthol and 1,3-dirnethylbarbiturie acid derivatives with using green condition through a simple, mild and efficient procedure utilizing cellulose sulfuric acid as a catalyst. Final compounds were evaluated for antibacterial and antifungal activity. Compounds 4a, 4d, 4h display high potent antifungal activity against Candida parapsilopsis, compound 4d show more potent activity (MIC 4.6 mg/mL) better than miconazole. While compound 4d most effective on bacterial against Micrococcus luteus, Staphylococcus aureus MTCC 96 and Staphylococcus aureus MTCC 2940 with (MIC 2.3 mg/mL).
机译:由偶联合成的一系列新的新颖的8,10-二甲基-12-芳基-12H-萘并[1',2,5,6]吡喃并[2,3-d]嘧啶-9,11-二酮衍生物(3CC)通过使用纤维素硫酸作为催化剂的简单,温和而有效的程序,通过绿色条件使用绿色条件制备醛,β-萘酚和1,3-己基巴比妥酸衍生物。评价最终化合物的抗菌和抗真菌活性。化合物4a,4d,4h对副孢霉念珠菌显示出高有效的抗真菌活性,化合物4d显示出比咪康唑更好的有效活性(MIC 4.6 mg / mL)。尽管化合物4d对细菌最有效的抗黄褐微球菌,金黄色葡萄球菌MTCC 96和金黄色葡萄球菌MTCC 2940(MIC 2.3 mg / mL)。

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