吴元鎏. 取代脲的合成及其体外抗菌作用J. 药学学报, 1965, 12(8): 523-532.
引用本文: 吴元鎏. 取代脲的合成及其体外抗菌作用J. 药学学报, 1965, 12(8): 523-532.
WU YUAN-LIU. THE PREPARATION OF SUBSTITUTED UREAS AND THEIR IN VITRO BACTERIOSTATIC ACTIVITYJ. Acta Pharmaceutica Sinica, 1965, 12(8): 523-532.
Citation: WU YUAN-LIU. THE PREPARATION OF SUBSTITUTED UREAS AND THEIR IN VITRO BACTERIOSTATIC ACTIVITYJ. Acta Pharmaceutica Sinica, 1965, 12(8): 523-532.

取代脲的合成及其体外抗菌作用

THE PREPARATION OF SUBSTITUTED UREAS AND THEIR IN VITRO BACTERIOSTATIC ACTIVITY

  • 摘要: 为寻找抗绿脓杆菌及抗金黄色葡萄球菌药物,合成了18个芳基取代脲、4-芳基氨脲及芳基双脲提供抗菌筛选.2-甲基-4-氨基-6-对溴苯脲基喹啉(18)对绿脓杆菌及1,3-双(对溴笨基)硫脲(1)对金黄色葡萄球菌的体外抗菌作用最强,最低抑菌浓度分别为8微克/毫升及低于1微克/毫升.

     

    Abstract: A number of substituted ureas (Ⅳ) and related intermediates were prepared. Their methods of preparation and physical data were described and tabulated in Table 1. The in vitro bacteriostatic activity of these compounds was tested against Pseudomonas aerug-inosa (PA) and Micrococcus pyogenes var. aureus (MPA) and the results were sum- marized in Tables 2 and 3. Compound 18 (Ⅳ, R1=Br, R2=(?),X=O), the most active against PA, inhibits the growth at a concentration of 8 micrograms per millilitre. Compound 1 (Ⅳ, R1=Br, R2=(?)-Br, X=S), the most active against MPA, inhibits the growth at a concentration less than one microgram per millilitre.

     

/

返回文章
返回