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Antimicrobial activity of new dumbbell-shaped phenothiazine cinnamides

机译:新哑铃形吩噻嗪的抗菌活性

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Herein, we report the synthesis and in vitro antibacterial and antifungal activities for twelve (E)-3-(10-(4-(10H-phenothiazin-10-yl)phenyl)-10H-phenothiazin-3-yl)-N-phenyl acrylamides (1-12). Structures of the compounds were established using IR, H-1 NMR, mass and elemental analysis. These compounds exhibited promising activity against bacterials rather than fungal strains used. All the compounds inhibited the Gram-negative E. coli (ATCC 25922) and compounds 3, 5, 7, 8 and 12 also inhibited Gram-negative Pseudomonas (ATCC 27853) species in nano molar concentrations. Disc diffusion and micro-dilution (for MIC) methods were employed in estimating their in vitro antibacterial and antifungal activities. Ciprofloxacin and ketoconazole were used as the respective internal standards.
机译:在此,我们报告了十二(E)-3-(10-(4-(10H-吩噻嗪-10-基)苯基)-10h-吩噻嗪-3-基)的合成和体外抗菌和抗真菌活性。-N- 苯基丙烯酰胺(1-12)。 使用IR,H-1 NMR,质量和元素分析建立化合物的结构。 这些化合物表现出对细菌的有希望的活性而不是使用的真菌菌株。 所有化合物抑制革兰氏阴性大肠杆菌(ATCC 25922)和化合物3,5,7,8和12也抑制纳米摩尔浓度的革兰氏阴性假鼠(ATCC 27853)物种。 在估计其体外抗菌和抗真菌活性时,使用盘扩散和微量稀释(用于MIC)方法。 使用环丙沙星和酮康唑作为各自的内标。

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