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Synthesis, Spectroscopic Characterization and Antibacterial Screening of Novel N-(Benzothiazol-2-yl)ethanamides

机译:新型N-(苯并噻唑-2-基)乙酰胺的合成,光谱表征和抗菌筛选

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Synthesis, electronic, infrared, elemental micro analytical studies were carried on N-(benzothiazol-2-yl)trichloroethanamide (4) and N-(benzothiazol-2-yl)chloroefhanamide (5). They were also screened in vitro and in vivo for antibacterial activity. The results indicate that the compounds are stable and that they show high antibacterial activities against both gram-positive and gram-negative bacteria tested. Both derivatives of 2-aminobenzothiazole were active against the multiresistant bacteria with diameter of inhibition zone ranging from 9-18 mm (5) and 9-20 mm (4). From the MIC results it is observed that the [5] derivative produced a better antibacterial activity than the (4) derivative. The lethal concentrations (LC_(50)) of the compounds were also determined. Their solubilities and melting points were also determined.
机译:对N-(苯并噻唑-2-基)三氯乙酰胺(4)和N-(苯并噻唑-2-基)氯乙酰胺(5)进行了合成,电子,红外,元素微观分析研究。还对它们的体外和体内抗菌活性进行了筛选。结果表明该化合物是稳定的,并且它们对所测试的革兰氏阳性和革兰氏阴性细菌均显示出高抗菌活性。 2-氨基苯并噻唑的两种衍生物均对多重耐药细菌具有活性,抑制区的直径范围为9-18 mm(5)和9-20 mm(4)。从MIC结果,观察到[5]衍生物比(4)衍生物产生更好的抗菌活性。还确定了化合物的致死浓度(LC_(50))。还确定了它们的溶解度和熔点。

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