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首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Synthesis and antibacterial activity of some novel 6-(1H-benz[d] imidazol-2-yl)-8-(5-nitro-2-furyl)-3-(4-pyridyl)-7,8-dihydro[1,2,4] triazolo[3,4-b][1,3,4]thiadiazepines
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Synthesis and antibacterial activity of some novel 6-(1H-benz[d] imidazol-2-yl)-8-(5-nitro-2-furyl)-3-(4-pyridyl)-7,8-dihydro[1,2,4] triazolo[3,4-b][1,3,4]thiadiazepines

机译:某些新型6-(1H-苯并[d]咪唑-2-基)-8-(5-硝基-2-呋喃基)-3-(4-吡啶基)-7,8-二氢[1]的合成​​及抑菌活性,2,4] triazolo [3,4-b] [1,3,4] thiadiazepines

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摘要

A new series of novel 6-(1H-benz[d]imidazol-2-yl)-8-(5-nitro-2-furyl)-3-(4- pyridyl)-7,8-dihydro[1,2,4]triazolo[ 3,4-b][1,3,4]thiadiazepines 8a - d has been synthesized. These compounds were evaluated for their efficiency as antibacterial agents against two Gram-positive and Gram-negative strains of bacteria along with anti-fungal activity against two fungal organisms. The antibacterial and antifungal activities of the present compounds were not comparable with those of the standard drugs employed. But, however, all the test compounds could exhibit notable activities only at higher concentrations (250, 500 μg/ml). The chemical structures of these compounds were confirmed on the basis of spectral data.
机译:一系列新的新型6-(1H-苯并[d]咪唑-2-基)-8-(5-硝基-2-呋喃基)-3-(4-吡啶基)-7,8-二氢[1,2合成了,4]三唑并[3,4-b] [1,3,4]噻二氮杂8a-d。评价了这些化合物作为针对两种革兰氏阳性和革兰氏阴性细菌的抗菌剂的功效以及对两种真菌生物的抗真菌活性。本发明化合物的抗菌和抗真菌活性与所用标准药物的抗菌和抗真菌活性不可比。但是,所有测试化合物只有在较高浓度(250、500μg/ ml)下才能表现出显着活性。根据光谱数据证实了这些化合物的化学结构。

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