首页> 外文期刊>Journal of Planar Chromatography-Modern TLC: JPC >Evaluation of the Lipophilicity and Prediction of BioSogical Activity of Some N-CycIohexyl-N-Substituted-2-Phenylacetamide Derivatives Using RP-TLC
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Evaluation of the Lipophilicity and Prediction of BioSogical Activity of Some N-CycIohexyl-N-Substituted-2-Phenylacetamide Derivatives Using RP-TLC

机译:使用RP-TLC评价某些N-环己基-N-取代的2-苯基乙酰胺衍生物的亲脂性并预测其生物化学活性

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摘要

The chromatographic behavior of N-cycIohexyl-N-substituted-2-phenylacetamides was investigated using reversed phase thin-layer chromatography (RP-TLC). RP-TLC was performed on a C-18 bonded phase with different aqueous eluents: water-acetone, water-acetonitrile and water-dioxane. Linear relationship between retention parameters and organic modifier content in the mobile phase allows the extrapolation procedure. From results, it is evident that retention behavior of investigated compound depended on structures of substituents R. The correlation between the chromatographic lipophilic parameters (R_M~0) and calculated log P values and several pharmacokinetics parameters such as HIA (human intestinal absorption) predictor, the plasma protein binding (PB) predictor, and partition predictor for predicting the biological activity of the blood-brain barrier (BBB) has been studied. The results show that reversed-phase R_M~0 proved to express lipophilic nature of investigated compounds as well as biological activity.
机译:使用反相薄层色谱法(RP-TLC)研究了N-环己基-N-取代-2-苯基乙酰胺的色谱行为。 RP-TLC在C-18键合相上使用不同的水洗脱液进行:水-丙酮,水-乙腈和水-二恶烷。流动相中保留参数和有机改性剂含量之间的线性关系允许外推程序。从结果可以明显看出,所研究化合物的保留行为取决于取代基R的结构。色谱亲脂性参数(R_M〜0)与计算出的log P值之间的相关性以及诸如HIA(人类肠道吸收)预测因子等几种药代动力学参数,已经研究了血浆蛋白结合(PB)预测因子和预测血脑屏障(BBB)生物学活性的分区预测因子。结果表明,反相R_M〜0被证明可以表达所研究化合物的亲脂性和生物活性。

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