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Lipophilicity analysis of newly synthetized quinobenzothiazines by use of TLC

机译:薄层色谱法分析新合成的喹啉苯并噻嗪的亲脂性

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Lipophilicity is a very important property of chemical compound taking into consideration in drugs design. Relationships between biological activity, among others lipophilicity, and chemical structure (QSAR) of the compound are very often used by researches. Especially important is the kind of substituents connected to the basic structural fragment and how it changes the lipophilicity of the compound. The aim of this study was to determine the parameters of lipophilicity of quinobenzothiazine derivatives using reversed phase - thin-layer chromatography (RP-TLC), which would enable one to determine the structure-activity relationship. The objective of our work is a series of 15 newly synthetized quinobenzothiazines. They were analyzed by thin-layer chromatography (TLC) with the use of two different mobile phases consisting of methanol or acetone as organic modifiers. For all compounds investigated, the values of lipophilicity obtained from computational method were also determined. Cluster analysis was carried out too for all data of lipophilicity obtained. Low correlation was found between values of experimental lipophilicity and lipophilicity from computational methods for newly synthetized compounds.
机译:亲脂性是在药物设计中考虑到的化合物的非常重要的性质。研究中经常使用生物活性(尤其是亲脂性)与化合物的化学结构(QSAR)之间的关系。与基本结构片段连接的取代基的种类及其如何改变化合物的亲脂性尤其重要。这项研究的目的是使用反相薄层色谱法(RP-TLC)确定喹啉苯并噻嗪衍生物的亲脂性参数,这将使人们能够确定其结构活性关系。我们的工作目标是一系列15种新合成的喹啉苯并噻嗪。通过使用由甲醇或丙酮组成的两种不同流动相作为有机改性剂的薄层色谱(TLC)分析它们。对于所有研究的化合物,还确定了通过计算方法获得的亲脂性值。对于获得的所有亲脂性数据也进行了聚类分析。通过新合成化合物的计算方法,发现实验亲脂性和亲脂性之间的相关性较低。

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