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新型硫代巴比妥酸衍生的螺杂双环化合物的合成及其抗菌活性。

Synthesis of new thiobarbituric acid derived spiroheterobicyclic compounds and their antimicrobial activity.

作者信息

Kaur Gurpreet, Gupta Parul, Harjai Kusum, Singh Vasundhara

机构信息

Department of Applied Sciences, PEC University of Technology, Chandigarh, 160012, India.

出版信息

Drug Dev Res. 2014 May;75(3):202-10. doi: 10.1002/ddr.21172. Epub 2014 Apr 15.

Abstract

A series pf novel (7S, 11R)-substituted diphenyl-2,4,8,10-tetraazaspiro [5.5] undecane-3-thio-1,5,9-triones 4a-j and (7S,11R)-substituted diphenyl-2,4,8,10-tetraazaspiro[5.5] undecane-3-thio-1,5 dione, 9-thiones 5a-j were prepared using substituted aldehydes and urea/thiourea in the presence of thiobarbituric acid under solvent free, thermal and microwave conditions catalyzed by ecofriendly K-10 clay. The antibacterial potency of these compounds in vitro on the gram negative strains Escherichia coli and Pseudomonas aeruginosa and gram positive strains Staphyllococcus aureus and Staphylococcus epidermidis was evaluated.

摘要

使用取代醛和尿素/硫脲,在无溶剂、热和微波条件下,以环保型K-10粘土为催化剂,在硫代巴比妥酸存在下,制备了一系列新型的(7S, 11R)-取代二苯基-2,4,8,10-四氮杂螺[5.5]十一烷-3-硫代-1,5,9-三酮4a-j和(7S,11R)-取代二苯基-2,4,8,10-四氮杂螺[5.5]十一烷-3-硫代-1,5-二酮、9-硫酮5a-j。评估了这些化合物对革兰氏阴性菌大肠杆菌和铜绿假单胞菌以及革兰氏阳性菌金黄色葡萄球菌和表皮葡萄球菌的体外抗菌效力。

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