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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, Raman, FT-IR, NMR spectroscopic data and antimicrobial activity of mixed aza-oxo-thia macrocyclic compounds.
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Synthesis, Raman, FT-IR, NMR spectroscopic data and antimicrobial activity of mixed aza-oxo-thia macrocyclic compounds.

机译:混合的氮杂-氧-硫杂大环化合物的合成,拉曼光谱,FT-IR,NMR光谱数据和抗菌活性。

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摘要

Mixed aza-oxo-thia macrocyclic ligands 1,3,5,11,13,15-hexaaza-6,10,16,20-tetraoxo-8,18-dithia-2,3,4:12,13,14-dipyridine cyclocosane (L(1)); 1,3,5,12,14,16-hexeaza-6,11,17,22-tetraoxo-8,9,19,20-tetrathia-2,3,4:13,14,15-dip yridine cyclodocosane (L(2)); 1,3,5,13,15,17-hexaaza-6,12,18,24-tetraoxo-9,21-dithia-2,3,4:14,15,16-dipyridine cyclotetracosane (L(3)) and 1,3,5,14,16,18-hexaaza-6,13,19,26-tetraoxo-9,10,22,23-tetrathia-2,3,4:15,16,17-di pyridine cyclohexacosane (L(4)) were synthesised. The structural features of the ligands have been studied by elemental analyses, Raman, IR, (1)H and (13)C NMR spectroscopy. The antimicrobial activities of the ligands were evaluated using disk diffusion method in dimethyl sulfoxide (DMSO) as well as the minimal inhibitory concentration (MIC) dilution method, against nine bacteria. The obtained results from disk diffusion method were assessed in side-by-side comparison with those of penicillin G, ampicillin, cefotaxime, vancomycin, ofloxacin, and tetracycline well known antibacterial agents. The results from dilution procedure were compared with gentamycin as antibacterial and nystatin as antifungal. The antifungal activities are reported on five yeast cultures namely Candida albicans, Kluyveromyces fragilis, Rhodotorula rubra, Debaryomyces hansenii, and Hanseniaspora guilliermondii, and the results are referenced with nystatin, Ketoconazole, and clotrimazole, commercial antifungal agents. In most cases, the compounds show broad-spectrum (Gram(+) and Gram(-) bacteria) activities that were more active or equipotent to the antibiotic and antifungal agents in the comparison tests.
机译:混合氮杂-氧-硫杂大环配体1,3,5,11,13,15-六氮杂-6,10,16,20-四氧-8,18-二硫杂-2,3,4:12,13,14-二吡啶环二十烷(L(1)); 1,3,5,12,14,16-己六-6,11,17,22-四氧8,9,19,20-四硫-2,3,4:13,14,15-二氢吡啶环二十二烷( L(2)); 1,3,5,13,​​15,17-hexaaza-6,12,18,24-tetraoxo-9,21-dithia-2,3,4:14,15,16-dipyridine cyclotetracosane(L(3))和1,3,5,14,16,18-hexaaza-6,13,19,26-tetraoxo-9,10,22,23-tetrathia-2,3,4:15,16,17-二吡啶环己烷(L(4))已合成。配位体的结构特征已通过元素分析,拉曼光谱,IR,(1)H和(13)C NMR光谱进行了研究。使用圆盘扩散法在二甲基亚砜(DMSO)中以及最小抑制浓度(MIC)稀释法中评估了9种细菌的配体的抗菌活性。通过圆盘扩散法获得的结果与青霉素G,氨苄青霉素,头孢噻肟,万古霉素,氧氟沙星和四环素众所周知的抗菌剂并排比较。将稀释过程的结果与庆大霉素作为抗菌剂和制霉菌素作为抗真菌剂进行比较。据报道有5种酵母培养物具有抗真菌活性,分别是白色念珠菌,脆弱克鲁维酵母,红红假单胞菌,汉逊Debaryomyces hansenii和Hanseniaspora guilliermondii,其结果以制霉菌素,酮康唑和克霉唑(商业抑菌剂)为参考。在大多数情况下,该化合物显示出广谱(革兰氏(+)和革兰氏(-)细菌)活性,在比较试验中这些活性对抗生素和抗真菌剂更具活性或等效。

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