首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Derivational, Structural, and Biological Studies of Some New Pyrazolyl, Isoxazolyl, Pyrimidinyl, Pyridazinyl, and Pyridopyridazinyl from 4-Substituted Antipyrine
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Derivational, Structural, and Biological Studies of Some New Pyrazolyl, Isoxazolyl, Pyrimidinyl, Pyridazinyl, and Pyridopyridazinyl from 4-Substituted Antipyrine

机译:一些新的吡唑基,异恶唑基,嘧啶基,哒嗪基,吡啶基吡啶基和4-取代的反紫蛋白的衍生物,结构和生物学研究

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摘要

(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)carbono-hydrazonoyl dicyanide was used as a key intermediate for the synthesis of novel pyrazole, isoxazole, pyrimidine, and pyridazine derivatives. The newly synthesized compounds were characterized by elemental analyses and spectral data (IR, H-1-NMR, C-13-NMR, and mass spectra). The compounds were tested for their in vitroantibacterial activity against Gram-positive bacteria as (Staphylococcus aureus and Bacillus subtilis) and Gram-negative bacteria (Pseudomonas aeruginosa and Escherichia coli). The investigated compounds were tested against two strains of fungi Botrytis fabae and Fusarium oxysporum using diffusion agar technique. The biological results showed clearly that most of the synthesized compounds revealed mild to moderate activity against the used microorganisms.
机译:(1,5-二甲基-3-氧代-2-苯基-2,3-二氢-1H-吡唑-4-基)羰基腙酰二腈是合成新型吡唑、异恶唑、嘧啶和哒嗪衍生物的关键中间体。通过元素分析和光谱数据(IR、H-1-NMR、C-13-NMR和质谱)对新合成的化合物进行了表征。测试了这些化合物对革兰氏阳性菌(金黄色葡萄球菌和枯草芽孢杆菌)和革兰氏阴性菌(铜绿假单胞菌和大肠杆菌)的体外抗菌活性。利用扩散琼脂技术对所研究的化合物进行了抗两株真菌蚕豆灰霉病菌和尖孢镰刀菌的试验。生物学结果清楚地表明,大多数合成的化合物显示出对所用微生物的轻度至中度活性。

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