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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, antimicrobial evaluation and QSAR study of some 3-hydroxypyridine-4-one and 3-hydroxypyran-4-one derivatives.
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Synthesis, antimicrobial evaluation and QSAR study of some 3-hydroxypyridine-4-one and 3-hydroxypyran-4-one derivatives.

机译:某些3-羟基吡啶-4-酮和3-羟基吡喃-4-酮衍生物的合成,抗菌评估和QSAR研究。

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摘要

A series of Mannich bases of 2-alkyl-3-hydroxy-pyridine-4-ones, namely 2-alkyl-3-hydroxy-5-N-piperidylmethyl or N,N-dialkylaminomethyl pyridine-4-ones 9, 10 and 15-18, two derivatives of N-aryl-2-methyl-3-hydroxy-pyridine-4-ones 19, 20 and two N-alkyl derivatives of maltol, 21 and 22 were prepared. They were screened for their antibacterial and antifungal activities against a variety of microorganisms using micro plate Alamar Blue((R)) assay (MABA) method. Multiple linear regressions (MLR) analysis was performed for the synthesized compounds as well as a series of pyridinone and pyranone derivatives 23-43 which have been synthesized and evaluated for antimicrobial activity by other researchers previously. Studied compounds showed a better quantitative structure-activity relationship (QSAR) model for the antimicrobial activity against Candida albicans and Staphylococcus aureus in comparison with other tested microorganisms.
机译:2-烷基-3-羟基吡啶-4-酮的一系列曼尼希碱,即2-烷基-3-羟基-5-N-哌啶基甲基或N,N-二烷基氨基甲基吡啶-4-酮9、10和15参照图-18,制备了N-芳基-2-甲基-3-羟基-吡啶-4-酮19、20的两个衍生物和麦芽酚21和22的两个N-烷基衍生物。使用微量培养板Alamar Blue(R)方法(MABA)筛选了它们对多种微生物的抗菌和抗真菌活性。对合成的化合物以及一系列嘧啶酮和吡喃酮衍生物23-43进行了多元线性回归(MLR)分析,这些化合物先前已被合成并已被其他研究人员评估了其抗菌活性。研究的化合物与其他测试微生物相比,对白色念珠菌和金黄色葡萄球菌的抗菌活性显示出更好的定量构效关系(QSAR)模型。

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