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Synthesis, Spectroscopic Studies and Antibacterial Activity of New Lauroyl Thiourea Amino Acid Derivatives

机译:新月桂酰硫脲氨基酸衍生物的合成,光谱研究和抗菌活性

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摘要

Four new thiourea compounds have been successfully synthesized and characterized from combination of lauroyl chloride, ammonium thiocyanate and simple amino acids in acetone. The structure of the respective compounds, namely 3-(3-dodecanoyl-thioureido)propionic acid (R1), 2-(3-dodecanoyl-thioureido)-3-methyl butyric acid (R2), (3-dodecanoyl-thioureido)acetic acid (R3) and 2-(3-dodecanoyI-thioureido)-3-phenyl propionic acid (R4) are confirmed by combination of spectroscopic techniques such as infrared, ultraviolet and nuclear magnetic resonance. The antibacterial activity of these compounds are investigated towards selected bacteria and the results show that compound R4 displays better antibacterial activity compared to R1-R3 and as well as to few reported compounds. Compound R4 shows good antibacterial activity towards two Gram-negative bacteria Escherichia coli and Salmonella typhitnurium. with inhibition zone approximately 8 mm wide and minimum inhibitory concentration (MIC) 50 μg/mL, respectively. The good results given by R4 might be attributed by the presence of alky] and phenyl group that increases the lipophilicity and stability of the compounds.
机译:从月桂酰氯,硫氰酸铵和简单氨基酸在丙酮中的组合,已经成功合成了四种新的硫脲化合物并对其进行了表征。相应化合物的结构,即3-(3-十二烷酰基-硫脲基)丙酸(R1),2-(3-十二烷酰基-硫脲基)-3-甲基丁酸(R2),(3-十二烷酰基-硫脲基)乙酸酸(R3)和2-(3-十二烷酰基-硫脲基)-3-苯基丙酸(R4)是通过结合光谱技术(例如红外,紫外和核磁共振)确定的。研究了这些化合物对选定细菌的抗菌活性,结果表明,与R1-R3和几乎没有报道的化合物相比,化合物R4具有更好的抗菌活性。化合物R4对两种革兰氏阴性细菌大肠杆菌和鼠伤寒沙门氏菌显示出良好的抗菌活性。抑菌圈宽约8毫米,最小抑菌浓度(MIC)分别为50μg/ mL。 R 4给出的良好结果可能归因于烷基和苯基的存在,它们增加了化合物的亲脂性和稳定性。

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