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Synthesis and biological activity studies of furan derivatives

机译:呋喃衍生物的合成及生物活性研究

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The organic compounds, 4-Ethyl-2,5,5-triphenyl-4,5-dihydrofuran-3-carbonitrile; 2,4,5-Triphenyl-5-propyl-4,5-dihydrofuran-3-carbonitrile; 4-Ethyl-5,5-diphenyl-2-thien-2-yl-4,5-dihydrofuran-3-carbonitrile; 2-(1-Benzofuran-2-yl-)-5-propyl-4,5-diphenyl-4,5-dihydrofuran-3-carbonitrile; 4-Ethyl-5,5-diphenyl-4,5-dihydro-2,2’-bifuran-3-carbonitrile, were synthesized and purified through column chromatography and preparative TLC. All compounds were characterized by IR, 1H, 13C NMR, MS, and microanalysis. The in vitro antibacterial and antifungal activities of these compounds were investigated against some bacteria and fungi. The antibacterial and antifungal activities were measured by using the disc-diffusion method against gram-positive bacteria, i.e., Staphylococcus aureus ATCC 25923, Staphylococcus enteritidis ATCC1376, Psydomamonas aeruginosa ATCC 29212, Bacillus subtilis RSKK 244, Bacillus megaterium gram-negative bacteria Escherichia coli ATCC 27853, Listeria monocytogenes ATCC 7644, and as fungus Micrococcus Luteus NRRLB was used. All compounds in this study showed activity against test bacteria. Their antibiogram tests showed better results than some known antibiotics.
机译:有机化合物4-乙基-2,5,5-三苯基-4,5-二氢呋喃-3-腈; 2,4,5-三苯基-5-丙基-4,5-二氢呋喃-3-腈; 4-乙基-5,5-二苯基-2-噻吩-2-基-4,5-二氢呋喃-3-腈; 2-(1-苯并呋喃-2-基-)-5-丙基-4,5-二苯基-4,5-二氢呋喃-3-腈;合成了4-乙基-5,5-二苯基-4,5-二氢-2,2'-联呋喃-3-腈,并通过柱色谱和制备型TLC纯化。所有化合物均通过IR, 1 H, 13 C NMR,MS和微量分析进行表征。研究了这些化合物对某些细菌和真菌的体外抗菌和抗真菌活性。通过圆盘扩散法对革兰氏阳性菌即金黄色葡萄球菌ATCC 25923,肠炎葡萄球菌ATCC1376,铜绿假单胞菌ATCC 29212,枯草芽孢杆菌RSKK 244,巨大芽孢杆菌ATCC革兰氏阴性菌进行了圆盘扩散法测定了其抗菌和抗真菌活性。 27853,单核细胞增生性李斯特菌ATCC 7644,并使用了黄曲霉微球菌NRRLB作为真菌。这项研究中的所有化合物均显示出对测试细菌的活性。他们的抗菌素检测结果显示比某些已知抗生素更好的结果。

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