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一些新型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[1,2,4]三唑并[3,4-b][1,3,4]噻二氮杂卓的合成与抗菌活性

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.

作者信息

Malla Reddy Vanga, Ravinder Reddy Kunduru

机构信息

Dr. Ch. Ravishanker Memorial Medicinal Chemistry Research Laboratory, University College of Pharmaceutical Sciences, Kakatiya University. Warangal, India.

出版信息

Chem Pharm Bull (Tokyo). 2010 Aug;58(8):1081-4. doi: 10.1248/cpb.58.1081.

Abstract

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 antifungal 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 microg/ml). The chemical structures of these compounds were confirmed on the basis of spectral data.

摘要

已合成了一系列新型的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[1,2,4]三唑并[3,4-b][1,3,4]噻二氮杂卓8a-d。对这些化合物作为抗菌剂针对两种革兰氏阳性和革兰氏阴性细菌菌株的效率以及针对两种真菌生物体的抗真菌活性进行了评估。本化合物的抗菌和抗真菌活性与所使用的标准药物不可比。但是,所有测试化合物仅在较高浓度(250、500微克/毫升)时才表现出显著活性。这些化合物的化学结构根据光谱数据得到了证实。

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