刘维勤, 崔起文. 抗綠脓杆菌药物的研究—9,10-二氮杂蒽类衍生物J. 药学学报, 1963, 10(11): 663-667.
引用本文: 刘维勤, 崔起文. 抗綠脓杆菌药物的研究—9,10-二氮杂蒽类衍生物J. 药学学报, 1963, 10(11): 663-667.
LIU WEI-CHIN AND TSUI CHI-WEN, . POTENTIAL ANTI-PSEUDOMONAS AERUGINOSA AGENTS PHENAZINESJ. Acta Pharmaceutica Sinica, 1963, 10(11): 663-667.
Citation: LIU WEI-CHIN AND TSUI CHI-WEN, . POTENTIAL ANTI-PSEUDOMONAS AERUGINOSA AGENTS PHENAZINESJ. Acta Pharmaceutica Sinica, 1963, 10(11): 663-667.

抗綠脓杆菌药物的研究—9,10-二氮杂蒽类衍生物

POTENTIAL ANTI-PSEUDOMONAS AERUGINOSA AGENTS PHENAZINES

  • 摘要: 据前人报告多粘菌素B具有抗绿脓杆菌的作用,是与该抗菌素的分子内含有五个游离氨基及脂溶性侧链有关的;另外有些9,10-二氮杂蒽类衍生物对不同株绿脓杆菌亦有抗菌作用.因此合成了一些取代氨基N-烷基-9,10-二氮杂蒽季胺盐,进行抗绿脓杆菌筛选,结果抗菌作用不明显.

     

    Abstract: The amino groups and the lipophilic side chain in polymyxin B have been reported to be responsible for the action against Pseudomonas aeruginosa. Since phenazine derivatives usually exhibited potent bacteriostatic action, we have accordingly prepared a number of phenazinium salts carrying amino groups and an N-alkyl side chain for screening purposes. However, antibacterial tests showed that none of the compounds so prepared was active.

     

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