Literature DB >> 8692723

Lipophilicity in molecular modeling.

B Testa1, P A Carrupt, P Gaillard, F Billois, P Weber.   

Abstract

PURPOSE: The molecular lipophilicity potential (MLP) offers a three-dimensional representation of lipophilicity, a molecular property encoding intermolecular recognition and intramolecular interactions.
METHOD: The interest and applications of the MLP in molecular modeling are varied, as illustrated here.
RESULTS: The MLP is a major tool to assess the dependence of lipophilicity on conformation. As a matter of fact, the MLP combined with an exploration of the conformational space of a solute reveals its "chameleonic" behavior, i.e. its capacity to adapt to its molecular environment by hydrophobic collapse or hydrophilic folding. Another successful application of the MLP is its concatenation into 3D-QSAR (Comparative Molecular Field Analysis, CoMFA).
CONCLUSION: Work is in progress to expand the MLP into a docking tool in the modeling of ligand-receptor interactions.

Mesh:

Year:  1996        PMID: 8692723     DOI: 10.1023/a:1016024005429

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  21 in total

1.  Production and characterization of 22 monoclonal antibodies directed against S 20499, a new potent 5-HT1A chiral agonist: influence of the hapten structure on specificity and stereorecognition.

Authors:  P Got; E Raimbaud; C Bussey; G Caron; P A Carrupt; B Walther; A Bensussan; J M Scherrmann
Journal:  Pharm Res       Date:  1999-05       Impact factor: 4.200

2.  Prediction of membrane permeability to peptides from calculated dynamic molecular surface properties.

Authors:  P Stenberg; K Luthman; P Artursson
Journal:  Pharm Res       Date:  1999-02       Impact factor: 4.200

3.  Identifying potential binding modes and explaining partitioning behavior using flexible alignments and multidimensional scaling.

Authors:  M Feher; J M Schmidt
Journal:  J Comput Aided Mol Des       Date:  2001-12       Impact factor: 3.686

Review 4.  Theoretical predictions of drug absorption in drug discovery and development.

Authors:  Patric Stenberg; Christel A S Bergström; Kristina Luthman; Per Artursson
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

5.  Quantitative structure-permeation relationships (QSPeRs) to predict skin permeation: a critical evaluation.

Authors:  Sandrine Geinoz; Richard H Guy; Bernard Testa; Pierre-Alain Carrupt
Journal:  Pharm Res       Date:  2004-01       Impact factor: 4.200

6.  The continuous molecular fields approach to building 3D-QSAR models.

Authors:  Igor I Baskin; Nelly I Zhokhova
Journal:  J Comput Aided Mol Des       Date:  2013-05-30       Impact factor: 3.686

7.  Prediction of intestinal drug absorption properties by three-dimensional solubility parameters.

Authors:  J Breitkreutz
Journal:  Pharm Res       Date:  1998-09       Impact factor: 4.200

8.  Predicting drug absorption from molecular surface properties based on molecular dynamics simulations.

Authors:  L H Krarup; I T Christensen; L Hovgaard; S Frokjaer
Journal:  Pharm Res       Date:  1998-07       Impact factor: 4.200

Review 9.  Stereoselectivity of antibodies for the bioanalysis of chiral drugs.

Authors:  P A Got; J M Scherrmann
Journal:  Pharm Res       Date:  1997-11       Impact factor: 4.200

10.  Computational approaches for modeling human intestinal absorption and permeability.

Authors:  Govindan Subramanian; Douglas B Kitchen
Journal:  J Mol Model       Date:  2006-04-01       Impact factor: 1.810

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