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- W2014610720 abstract "Abstract In recent times there has been a growing interest in the determination of chromatographic parameters of lipophilicity with regard to their use in the study of quantitative structure-activity relationship (1, 2). Very good correlations had been shown between the chromatographic parameters and the log P or π values as a measure of the partition coefficient between octanol and water (2). The reversed phase TLC Rm values in two different chromatographic systems and the reversed-phase HPLC log k′ values of a series of dermorphin-related oligopeptides have been previously determined (3, 4). The purpose of the present work was to study the relationship between log k′ values on one hand and Rm or Σπ values on the other one in view of QSAR studies. In fact the discovery of enkephalin and endorphins with high affinities for opioid receptors added new dimensions to the study of structure-activity relationship of opioid agonists (5, 6, 7, 8)." @default.
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- W2014610720 date "1984-06-01" @default.
- W2014610720 modified "2023-09-24" @default.
- W2014610720 title "Determination of Lipophilic Character of a Series of Dermorphin-Related Oligopeptioes by Means of Reversed-Phase HPLC" @default.
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- W2014610720 doi "https://doi.org/10.1080/01483918408074061" @default.
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