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Study of lipophilicity and membrane partition of 4-hydroxycoumarins by HPLC and PCA (CROSBI ID 188920)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Ilijaš, Marina ; Malnar, Ivica ; Gabelica Marković, Vesna ; Stepanić, Višnja Study of lipophilicity and membrane partition of 4-hydroxycoumarins by HPLC and PCA // Journal of pharmaceutical and biomedical analysis, 76 (2013), 104-111. doi: 10.1016/j.jpba.2012.11.043

Podaci o odgovornosti

Ilijaš, Marina ; Malnar, Ivica ; Gabelica Marković, Vesna ; Stepanić, Višnja

engleski

Study of lipophilicity and membrane partition of 4-hydroxycoumarins by HPLC and PCA

Physicochemical properties provide reliable guidance in optimization of pharmacological efficiency and ADME profile of small chemical compounds. Their high-throughput determination is regularly based on application of HPLC techniques. In this study CHI and CHI IAM of 32 4-hydroxycoumarin analogs were measured by HPLC with methanol gradient at pHs 2.8 and 7.0. Results were analyzed by PCA in terms of computed descriptors in order to identify space for optimization of their phospholipids affinity and lipophilicity for which predictive software failed to produce reliable estimations. The chromatographic behavior of studied 4-hydroxycoumarins was typical of acidic compounds. The CHI2.8, CHI7.0, CHI IAM2.8 and CHI IAM7.0 values were all considerably cross-correlated in accordance with their prevailing lipophilic character. Structure–retention relationship (SRR) analysis furthermore revealed that H-bond accepting capacity and dipolar interactions with methanol generally shorten their retention times. However, deviations from the linear trends were noticed for R3/R5-substituted derivatives able to form intramolecular contacts with the 4-O(H) group and characterized by more uniform electron density at 2-O and 4-O atoms and quite different acidity/H-bond donating capacity than the rest of derivatives. Thus, CHI and CHI IAM determinations and SRR analysis fast and efficiently pointed to ways of modifying biological activities of 4-hydroxycoumarins.

4-hydroxycoumarins; HPLC; CHI; CHI IAM; structure-retention reletaionship

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Podaci o izdanju

76

2013.

104-111

objavljeno

0731-7085

10.1016/j.jpba.2012.11.043

Povezanost rada

Kemija, Farmacija

Poveznice
Indeksiranost