首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and antimicrobial activity of some new thiazole, thiophene and pyrazole derivatives containing benzothiazole moiety.
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Synthesis and antimicrobial activity of some new thiazole, thiophene and pyrazole derivatives containing benzothiazole moiety.

机译:一些含有苯并噻唑部分的新噻唑,噻吩和吡唑衍生物的合成和抑菌活性。

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摘要

In an attempt to find a new class of antimicrobial agents, a series of thiazole, thiophene, pyrazole and other related products containing benzothiazole moiety were prepared via the reaction of N-(benzothiazol-2-yl)-2-cyanoacetamide (1) with appropriate chemical reagents. These compounds were screened for their antibacterial activity against gram-positive bacteria (Staphylococcus aureus and Streptococcus pyogenes), gram-negative bacteria (Pseudomonas phaseolicola and Pseudomonas fluorescens) and antifungal activity against Fusarium oxysporum and Aspergillus fumigatus. Among the synthesized compounds, thiophene 13 showed equal activity with chloroamphenicol against S. aureus (MIC 3.125 microg/mL), while its activity was 50% lower than of chloroamphenicol against S. pyogenes. Thiazole 3 and pyrazolo[1,5-a]pyrimidine 21 b were found to exhibit the most potent in vitro antifungal activity with MICs (6.25 microg/mL) against A. fumigatus and F. oxysporum. Structures of the newly synthesized compounds were established by elemental analysis and spectral data.
机译:为了寻找一类新型的抗菌剂,通过N-(苯并噻唑-2-基)-2-氰基乙酰胺(1)与N-(苯并噻唑-2-基)-2-氰基乙酰胺的反应制备了一系列噻唑,噻吩,吡唑和其他含有苯并噻唑部分的相关产品。适当的化学试剂。筛选了这些化合物对革兰氏阳性菌(金黄色葡萄球菌和化脓性链球菌),革兰氏阴性菌(Pseudomonas phaseolicola和Pseudomonas fluorescens)的抗菌活性以及对尖孢镰刀菌和烟曲霉的抗真菌活性。在合成的化合物中,噻吩13与氯霉素对金黄色葡萄球菌的活性相同(MIC 3.125 microg / mL),但其活性比对氯霉素对化脓性链球菌的活性低50%。噻唑3和吡唑并[1,5-a]嘧啶21b被发现具有最有效的体外抗真菌活性,MICs(6.25 microg / mL)对烟曲霉和尖孢镰刀菌具有抑制作用。通过元素分析和光谱数据确定了新合成化合物的结构。

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