4.4 Article

Determination of lipophilicity of α-(4-phenylpiperazine) derivatives of N-benzylamides using chromatographic and computational methods

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BIOMEDICAL CHROMATOGRAPHY
卷 22, 期 4, 页码 428-432

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WILEY
DOI: 10.1002/bmc.951

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lipophilicity; RP-TLC and HPLC; retention parameters R-M0; log k(0) capacity factors; calculated partition coefficient; N-benzylamides; derivatives of 4-phenylpiperazine

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This paper describes the evaluation of lipophilicity of alpha-(4-phenylpiperazine) derivatives of N-benzylamides. We employed reversed-phase thin-layer chromatography (RP-TLC) and reversed-phase high performance liquid chromatography (RP-HPLC) as experimental methods, using mixtures of acetonitrile and water as the mobile phases with addition of 0.1% TFA in the HPLC experiments. Retention parameters (R-M) and capacity factors (log k) determined by applying these methods were linearly dependent on the acetonitrile concentration and enabled us to estimate the relative lipophilicity factors: R-M0 and log k(0). These factors were compared with the calculated partition coefficients C log P obtained using several software packages. The results indicate that both experimental methods (RP-TLC and RP-HPLC) yielded similar results, and these methods enable determining the lipophilicity of alpha-(4-phenylpiperazine) derivatives of N-benzylamides. Significant correlations were found between log P values calculated by Pallas, ALOGPS and C log P Chem3D programs and the experimental data. Copyright (c) 2007 John Wiley & Sons, Ltd.

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