Determination of lipophilic descriptors of antihelmintic 6,7-diaryl-pteridine derivatives useful for bioactivity predictions.

The liquid chromatographic retention factors extrapolated to pure water, k'(w), for several 6,7-diaryl-pteridine derivatives in both an octadecylsilane (ODS) and an immobilized artificial membrane column (IAM.PC.DD2), using acetonitrile-aqueous buffer pH = 7.45 as mobile phase, were obtained. The logarithms of the k'(w) values in the IAM.PC.DD2 column, log k'(w) (IAM), show good correlation with the calculated values of the octanol-water partition coefficients, log P(o/w), showing that the chromatographic parameter can be used as lipophilicity descriptor for the studied pteridines. However, interactions other than the lipophilic ones seem to be involved in the ODS column. Previous studies have shown that pteridines have antihelmintic properties. In spite of the complexity of the studied biological system as compared with the chromatographic one, good correlation between the descriptors obtained in the IAM column and biological activity (expressed as the log of the inhibitory concentration required to obtain up to 50% in the reduction of population growth of nematodes, log IC(50)) was observed.

[1]  C. Poole,et al.  Retention characteristics of an immobilized artificial membrane column in reversed-phase liquid chromatography. , 2002, Journal of chromatography. A.

[2]  B. Smart Fluorine substituent effects (on bioactivity) , 2001 .

[3]  U. Norinder,et al.  The applicability of computational chemistry in the evaluation and prediction of drug transport properties , 2000 .

[4]  M. Abraham,et al.  Rapid-gradient HPLC method for measuring drug interactions with immobilized artificial membrane: comparison with other lipophilicity measures. , 2000, Journal of pharmaceutical sciences.

[5]  R. Kaliszan,et al.  Retention of barbituric acid derivatives on immobilized artificial membrane stationary phase and its correlation with biological activity. , 2000, Biomedical chromatography : BMC.

[6]  J. Silber,et al.  Role of Weak Molecular Interactions in the Mechanism of Action of a Series of Antihelmintics , 2000 .

[7]  S. Goldstein,et al.  IAM retention and blood brain barrier penetration , 1998 .

[8]  G. Caldwell,et al.  Evaluation of the immobilized artificial membrane phosphatidylcholine. Drug discovery column for high-performance liquid chromatographic screening of drug-membrane interactions. , 1998, Journal of chromatography. A.

[9]  M. Abraham,et al.  Relationships between the chromatographic hydrophobicity indices and solute descriptors obtained by using several reversed-phase, diol, nitrile, cyclodextrin and immobilised artificial membrane-bonded high-performance liquid chromatography columns , 1998 .

[10]  M. L. La Rotonda,et al.  Interactions of nonsteroidal antiinflammatory drugs with phospholipids: comparison between octanol/buffer partition coefficients and chromatographic indexes on immobilized artificial membranes. , 1997, Journal of pharmaceutical sciences.

[11]  C. Pidgeon,et al.  Predicting drug-membrane interactions by HPLC: structural requirements of chromatographic surfaces. , 1995, Analytical chemistry.

[12]  J. Silber,et al.  Competition between inter- and intramolecular hydrogen bonding in molecules with donor and acceptor groups. Solvatochromic and thermochromic evidence in n-(nitrophenyl)alkylenediamines , 1994 .

[13]  Lloyd R. Snyder,et al.  Retention in reversed-phase liquid chromatography as a function of mobile-phase composition , 1993 .

[14]  W. J. Lambert Modeling oil-water partitioning and membrane permeation using reversed-phase chromatography , 1993 .

[15]  M. Khaledi,et al.  Hydrophobicity estimations by reversed-phase liquid chromatography. Implications for biological partitioning processes. , 1993, Journal of chromatography.

[16]  J. Dorsey,et al.  Accurate determination of log k'w in reversed-phase liquid chromatography. Implications for quantitative structure-retention relationships. , 1993, Journal of chromatography.

[17]  Gerald J. Niemi,et al.  Optimal characterization of structure for prediction of properties , 1990 .

[18]  J. Dorsey,et al.  Estimation of the reversed-phase liquid chromatographic lipophilicity parameter log k'w using ET-30 solvatochromism. , 1990, Journal of chromatography.

[19]  M. Stud,et al.  High-Performance Liquid Chromatography of 1, 2, 6-Thiadiazinone 1, 1-Dioxides and Related Pyrazolones: A Comparative Study of Hydrophobicity , 1988 .

[20]  J. Legendre,et al.  Factors governing the retention of solutes on chromatographic immobilized artificial membranes : Application to anti-inflammatory and analgesic drugs , 1999 .

[21]  Ana Martínez,et al.  Comparative Molecular Field Analysis (CoMFA) on [6] + [6] Fused Pyrazines with Nematocide Properties , 1997 .

[22]  F. Quaglia,et al.  Chromatographic indices determined on an immobilized artificial membrane (IAM) column as descriptors of lipophilic and polar interactions of 4-phenyldihydropyridine calcium-channel blockers with biomembranes† , 1996 .

[23]  J. Dorsey,et al.  Bioavailability estimation by reversed-phase liquid chromatography: high bonding density C-18 phases for modeling biopartitioning processes. , 1995, Analytical chemistry.

[24]  C. Foces-Foces,et al.  Tautomerism in Pyrazino[2,3-c]-1,2,6-thiadiazine 2,2-Dioxides , 1988 .