赵临襄, 姚庆祥. N2-芳基三嗪青霉素和N2-苯基-N4-烷基(芳基)三嗪青霉素的合成及其抗菌活性J. 药学学报, 1990, 25(10): 739-744.
引用本文: 赵临襄, 姚庆祥. N2-芳基三嗪青霉素和N2-苯基-N4-烷基(芳基)三嗪青霉素的合成及其抗菌活性J. 药学学报, 1990, 25(10): 739-744.
LX Zhao, QX Yao. SYNTHESIS OF N2-ARYL - TRIAZINOYLAMOXICILLINS AND N2-PHENYL - N4- ALKYL ( ARYL )- TRIAZINOYLAMOXICILLINS AND THEIR ANTIBACTEBIAL ACTIVITYJ. Acta Pharmaceutica Sinica, 1990, 25(10): 739-744.
Citation: LX Zhao, QX Yao. SYNTHESIS OF N2-ARYL - TRIAZINOYLAMOXICILLINS AND N2-PHENYL - N4- ALKYL ( ARYL )- TRIAZINOYLAMOXICILLINS AND THEIR ANTIBACTEBIAL ACTIVITYJ. Acta Pharmaceutica Sinica, 1990, 25(10): 739-744.

N2-芳基三嗪青霉素和N2-苯基-N4-烷基(芳基)三嗪青霉素的合成及其抗菌活性

SYNTHESIS OF N2-ARYL - TRIAZINOYLAMOXICILLINS AND N2-PHENYL - N4- ALKYL ( ARYL )- TRIAZINOYLAMOXICILLINS AND THEIR ANTIBACTEBIAL ACTIVITY

  • 摘要: 设计合成了十个N2-芳基三嗪青霉素和六个N2-苯基-N4-烷基(芳基)三嗪青霉素,这十六个化合物均为未见文献报道的新化合物,元素分析数据和光谱数据证实了它们的结构。初步体外抑菌试验表明,十六个化合物对G(+)菌和G(-)菌均有一定的活性,其中的五个化合物具有一定程度的广谱特征。

     

    Abstract: Sixteen derivatives of BL-P1908 were synthesized by reaction of 2-aryl-1, 2, 4-triazine-3, 5-dione-6-carboxylic acid, or 2-phenyl-4-alkyl (aryl)-1, 2, 4-triazine-3, 5-dione-6-carboxylic acid with amoxicillin. All of them are new compounds. Their chemical structures were determined by elemental analysis, IR and 1HNMR. Preliminary tests showed that all compounds have marked activities agairist standard G(+) and G(-) bacteria and five of them have certain characteristic of broad spectrum, but they have no activities against resistant strains S. aureus S1, E coli C1 and P. aeruginosa PS1 isolated from clinic.

     

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