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首页> 外文期刊>Archiv der Pharmazie >Synthesis of some oxime ether derivatives of 1-(2-naphthyl)-2-(1,2,4-triazol-1-yl)ethanone and their anticonvulsant and antimicrobial activities.
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Synthesis of some oxime ether derivatives of 1-(2-naphthyl)-2-(1,2,4-triazol-1-yl)ethanone and their anticonvulsant and antimicrobial activities.

机译:1-(2-萘基)-2-(1,2,4-三唑-1-基)乙酮的肟肟衍生物的合成及其抗惊厥和抗菌活性。

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In this study, oxime and oxime ether derivatives of [1-(2-naphthyl)-2-(1,2,4-triazol-1-yl)ethanone] were prepared as potential anticonvulsant and antimicrobial compounds. The oxime was synthesized by the reaction of ketone and hydroxylamine hydrochloride. O-Alkylation of the oxime by various alkyl halides gave the oxime ether derivatives. Anticonvulsant activity of the compounds was determined by maximal electroshock and subcutaneous metrazole tests in mice and rats according to procedures of the Anticonvulsant Screening Program of National Institutes of Health. Neurotoxicity was determined by the rotorod test in mice and the positional sense test, gait and stance test in rats. In addition to anticonvulsant tests, all compounds were also evaluated against the following microorganisms: S. aureus, E. coli, P. aeruginosa, E. faecalis, C. albicans, C. parapsilosis, and C. krusei using microdilution broth method for possible antibacterial and antifungal activities. Although most of the O-alkyl substituted oxime ethers exhibited both anticonvulsant and antimicrobial activities, the O-arylalkyl substituted compounds were found to be inactive in both screening paradigms.
机译:在这项研究中,[1-(2-萘基)-2-(1,2,4-三唑-1-基)乙酮的肟和肟醚衍生物被制备为潜在的抗惊厥药和抗菌化合物。肟是通过酮与盐酸羟胺反应合成的。通过各种烷基卤对肟进行O-烷基化反应,得到肟醚衍生物。根据美国国立卫生研究院抗惊厥筛选计划的程序,通过在小鼠和大鼠中进行最大的电击和皮下甲唑试验,确定化合物的抗惊厥活性。通过在小鼠中的旋翼试验和在大鼠中的位置感觉试验,步态和姿势试验确定神经毒性。除抗惊厥试验外,还使用微量稀释液法对所有化合物针对以下微生物进行了评估:金黄色葡萄球菌,大肠杆菌,铜绿假单胞菌,粪肠球菌,白色念珠菌,副念珠菌和克鲁氏梭菌。抗菌和抗真菌活性。尽管大多数O-烷基取代的肟醚均表现出抗惊厥和抗菌活性,但发现O-芳基烷基取代的化合物在两种筛选范例中均无活性。

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