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Evaluation of the human prediction of clearance from hepatocyte and microsome intrinsic clearance for 52 drug compounds

Xenobiotica, 2010-09, Vol.40 (9), p.637-649

2010

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Melanocortin Receptors: Ligands and Proteochemometrics Modeling

Annals of the New York Academy of Sciences, 2003-06, Vol.994 (1), p.21-26

2003

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Improved approach for proteochemometrics modeling: application to organic compound—amine G protein-coupled receptor interactions

Bioinformatics, 2005-12, Vol.21 (23), p.4289-4296

2005

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New aspects on the melanocortins and their receptors

Pharmacological research, 2000-11, Vol.42 (5), p.393-420

2000

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A Three-Dimensional Model for the Interaction of MSH with the Melanocortin-1 Receptor

Biochemical and biophysical research communications, 1995-05, Vol.210 (1), p.205-210

1995

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Evidence for Alternate Points of Attachment for α-MSH and Its Stereoisomer (Nle4,D-Phe7)-α-MSH at the Melanocortin-1 Receptor

Biochemical and biophysical research communications, 1994-08, Vol.202 (3), p.1266-1271

1994

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Development of proteo-chemometrics: a novel technology for the analysis of drug-receptor interactions

Biochimica et biophysica acta, 2001-02, Vol.1525 (1), p.180-190

2001

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Proteochemometrics Modeling of the Interaction of Amine G-Protein Coupled Receptors with a Diverse Set of Ligands

Molecular pharmacology, 2002-06, Vol.61 (6), p.1465-1475

2002

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Classification of G‐protein coupled receptors by alignment‐independent extraction of principal chemical properties of primary amino acid sequences

Protein science, 2002-04, Vol.11 (4), p.795-805

2002

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Prediction of indirect interactions in proteins

BMC bioinformatics, 2006-03, Vol.7 (1), p.167-167, Article 167

2006

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Unbiased descriptor and parameter selection confirms the potential of proteochemometric modelling

BMC bioinformatics, 2005-03, Vol.6 (1), p.50-50, Article 50

2005

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Rough set-based proteochemometrics modeling of G-protein-coupled receptor-ligand interactions

Proteins, structure, function, and bioinformatics, 2006-04, Vol.63 (1), p.24-34

2006

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Proteochemometric Mapping of the Interaction of Organic Compounds with Melanocortin Receptor Subtypes

Molecular pharmacology, 2005-01, Vol.67 (1), p.50-59

2005

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QSAR and Proteo-chemometric Analysis of the Interaction of a Series of Organic Compounds with Melanocortin Receptor Subtypes

Journal of medicinal chemistry, 2003-06, Vol.46 (13), p.2572-2579

2003

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Proteochemometric modelling of antibody–antigen interactions using SPOT synthesised peptide arrays

Protein engineering, design and selection, 2007-06, Vol.20 (6), p.301-307

2007

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Synthesis and Quantitative Structure−Activity Relationship of Hydrazones of N-Amino-N‘-hydroxyguanidine as Electron Acceptors for Xanthine Oxidase

Journal of medicinal chemistry, 2004-06, Vol.47 (12), p.3105-3110

2004

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Proteo-chemometrics analysis of MSH peptide binding to melanocortin receptors

Protein engineering, 2002-04, Vol.15 (4), p.305-311

2002

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Long term orexigenic effect of a novel melanocortin 4 receptor selective antagonist

British journal of pharmacology, 1999-01, Vol.126 (1), p.27-34

1999

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Selectivity of Cyclic [d-Nal7] and [d-Phe7] Substituted MSH Analogues for the Melanocortin Receptor Subtypes

Peptides (New York, N.Y. : 1980), 1997, Vol.18 (7), p.1009-1013

1997

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Modeling of the three-dimensional structure of the human melanocortin 1 receptor, using an automated method and docking of a rigid cyclic melanocyte-stimulating hormone core peptide

Journal of molecular graphics & modelling, 1997-10, Vol.15 (5), p.307-317

1997

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Design of new small cyclic melanocortin receptor-binding peptides using molecular modelling: Role of the His residue in the melanocortin peptide core

European journal of medicinal chemistry, 2001-02, Vol.36 (2), p.137-146

2001

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PLS modeling of chimeric MS04/MSH-peptide and MC1/MC3-receptor interactions reveals a novel method for the analysis of ligand-receptor interactions

Biochimica et biophysica acta, 2001-01, Vol.1544 (1-2), p.350-357

2001

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Binding of cyclic and linear MSH core peptides to the melanocortin receptor subtypes

European journal of pharmacology, 1997-01, Vol.319 (2), p.369-373

1997

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Selective properties of C- and N-terminals and core residues of the melanocyte-stimulating hormone on binding to the human melanocortin receptor subtypes

European journal of pharmacology, 1998-05, Vol.349 (2), p.359-366

1998

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Thyrotropin releasing hormone (TRH) selectively binds and activates the melanocortin 1 receptor

Peptides (New York, N.Y. : 1980), 1999-01, Vol.20 (3), p.395-400

1999

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Evaluation of the human prediction of clearance from hepatocyte and microsome intrinsic clearance for 52 drug compounds

Melanocortin Receptors: Ligands and Proteochemometrics Modeling

Improved approach for proteochemometrics modeling: application to organic compound—amine G protein-coupled receptor interactions

New aspects on the melanocortins and their receptors

A Three-Dimensional Model for the Interaction of MSH with the Melanocortin-1 Receptor

Evidence for Alternate Points of Attachment for α-MSH and Its Stereoisomer (Nle4,D-Phe7)-α-MSH at the Melanocortin-1 Receptor

Development of proteo-chemometrics: a novel technology for the analysis of drug-receptor interactions

Proteochemometrics Modeling of the Interaction of Amine G-Protein Coupled Receptors with a Diverse Set of Ligands

Classification of G‐protein coupled receptors by alignment‐independent extraction of principal chemical properties of primary amino acid sequences

Prediction of indirect interactions in proteins

Unbiased descriptor and parameter selection confirms the potential of proteochemometric modelling

Rough set-based proteochemometrics modeling of G-protein-coupled receptor-ligand interactions

Proteochemometric Mapping of the Interaction of Organic Compounds with Melanocortin Receptor Subtypes

QSAR and Proteo-chemometric Analysis of the Interaction of a Series of Organic Compounds with Melanocortin Receptor Subtypes

Proteochemometric modelling of antibody–antigen interactions using SPOT synthesised peptide arrays

Synthesis and Quantitative Structure−Activity Relationship of Hydrazones of N-Amino-N‘-hydroxyguanidine as Electron Acceptors for Xanthine Oxidase

Proteo-chemometrics analysis of MSH peptide binding to melanocortin receptors

Long term orexigenic effect of a novel melanocortin 4 receptor selective antagonist

Selectivity of Cyclic [d-Nal7] and [d-Phe7] Substituted MSH Analogues for the Melanocortin Receptor Subtypes

Modeling of the three-dimensional structure of the human melanocortin 1 receptor, using an automated method and docking of a rigid cyclic melanocyte-stimulating hormone core peptide

Design of new small cyclic melanocortin receptor-binding peptides using molecular modelling: Role of the His residue in the melanocortin peptide core

PLS modeling of chimeric MS04/MSH-peptide and MC1/MC3-receptor interactions reveals a novel method for the analysis of ligand-receptor interactions

Binding of cyclic and linear MSH core peptides to the melanocortin receptor subtypes

Selective properties of C- and N-terminals and core residues of the melanocyte-stimulating hormone on binding to the human melanocortin receptor subtypes

Thyrotropin releasing hormone (TRH) selectively binds and activates the melanocortin 1 receptor

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