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Synthesis of novel dopamine derived multidirectional ligands from cyanuric chloride: structural and antimicrobial studies

机译:氰尿酰氯合成新型多巴胺衍生的多向配体:结构和抗菌研究

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摘要

Two monopodal (2,4-dichloro-6-(3-hydroxytyramine)-1,3,5-triazine) and tripodal (2,4,6-(3-hydroxytyramine)-1,3,5-triazine) s-triazine derivatives were prepared through the reaction of cyanuric chloride (2,4,6-trichloro-1,3,5-triazine) and 3-hydroxytyramine hydrochloride (dopamine hydrochloride). The structures of the compounds were identified by FT-IR, 1H NMR, 13C NMR, thermal analysis and elemental analysis. Their antimicrobial activities were carried out using the broth microdilution method in dimethyl sulfoxide (DMSO): Phosphate Buffered Saline (PBS) against eight bacteria and one yeast. The results of the test were compared with ampicillin. It was determined that CCDOP1, CCDOP3 and DOP have significant antibacterial and antifungal activity. These three chemicals revealed strong antibacterial activity against the E. coli and S. aureus strains used in the study. S. aureus was the most sensitive strain against dopamine hydrochloride and E. coli was the most sensitive bacteria against CCDOP1.
机译:两个单足(2,4-dichloro-6-(3-hydroxytyramine)-1,3,5-triazine)和三脚架(2,4,6-(3-hydroxytramine)-1,3,5-triazine)s-三嗪衍生物是通过氰尿酰氯(2,4,6-三氯-1,3,5-三嗪)和3-羟基酪胺盐酸盐(多巴胺盐酸盐)反应制得的。通过FT-IR,1 H NMR,13 C NMR,热分析和元素分析鉴定化合物的结构。使用肉汤微稀释法在二甲基亚砜(DMSO):磷酸盐缓冲盐水(PBS)中对8种细菌和1种酵母进行了抗菌活性测定。测试结果与氨苄西林进行了比较。已确定CCDOP1,CCDOP3和DOP具有显着的抗菌和抗真菌活性。这三种化学物质对研究中使用的大肠杆菌和金黄色葡萄球菌菌株显示出强大的抗菌活性。金黄色葡萄球菌是对盐酸多巴胺最敏感的菌株,而大肠杆菌是对CCDOP1最敏感的细菌。

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