Vai al contenuto principale della pagina

Molecular Interaction Fields [[electronic resource] ] : Applications in Drug Discovery and ADME Prediction



(Visualizza in formato marc)    (Visualizza in BIBFRAME)

Autore: Cruciani Gabriele Visualizza persona
Titolo: Molecular Interaction Fields [[electronic resource] ] : Applications in Drug Discovery and ADME Prediction Visualizza cluster
Pubblicazione: Hoboken, : Wiley, 2006
Descrizione fisica: 1 online resource (323 p.)
Disciplina: 615.19
Soggetto topico: Biomolecules
Chemical reactions -- Computer simulation
Chemicals -- Pharmacokinetics -- Forecasting
Chemicals -- Physiological effect -- Forecasting
Drug development
Pharmaceutical chemistry
Structure-activity relationships (Biochemistry) -- Computer simulation
Pharmaceutical chemistry - Physiological effect - Forecasting
Chemicals - Computer simulation
Chemical reactions - Computer simulation
Structure-activity relationships (Biochemistry)
Computational Biology
Models, Molecular
Quantitative Structure-Activity Relationship
Computer Simulation
Drug Design
Pharmaceutical Preparations
Software
Structure-Activity Relationship
Biology
Drug Discovery
Computing Methodologies
Chemicals and Drugs
Models, Theoretical
Biological Science Disciplines
Chemistry, Pharmaceutical
Biochemical Phenomena
Information Science
Pharmacological Phenomena
Investigative Techniques
Natural Science Disciplines
Analytical, Diagnostic and Therapeutic Techniques and Equipment
Pharmacology
Physiological Phenomena
Chemistry
Chemical Phenomena
Phenomena and Processes
Disciplines and Occupations
Pharmacy, Therapeutics, & Pharmacology
History of Medicine
Health & Biological Sciences
Medicine
Altri autori: MannholdRaimund  
KubinyiHugo  
FolkersGerd  
Note generali: Description based upon print version of record.
Nota di contenuto: Molecular Interaction Fields; A Personal Foreword; Contents; Preface; List of Contributors; I Introduction; 1 The Basic Principles of GRID; 1.1 Introduction; 1.2 Philosophy and Objectives; 1.3 Priorities; 1.4 The GRID Method; 1.4.1 GRID Probes Are Anisometric; 1.4.2 The Target "Responds" to the Probe; 1.4.3 The Target is Immersed in Water; 1.5 The GRID Force Field; 1.5.1 The Lennard-Jones Term; 1.5.2 The Electrostatic Term; 1.5.3 The Hydrogen Bond Term; 1.5.4 The Other Terms; 1.6 Nomenclature; 1.6.1 "ATOM" Records; 1.6.2 "HETATM" Records; 1.7 Calibrating the GRID Force Field
1.7.1 Checking the Calibration1.7.2 Checking Datafile GRUB; 1.8 The Output from GRID; 1.8.1 GRID Maps from Macromolecules; 1.8.2 GRID Maps from a Small Molecule; 1.9 Conclusions; 2 Calculation and Application of Molecular Interaction Fields; 2.1 Introduction; 2.2 Calculation of MIFs; 2.2.1 The Target; 2.2.2 The Probe; 2.2.3 The Interaction Function; 2.2.3.1 Van der Waals Interactions; 2.2.3.2 Electrostatic Interactions; 2.2.3.3 Hydrogen Bonds; 2.2.3.4 Entropy; 2.3 Selected Applications of MIFs; 2.3.1 Mapping a Ligand Binding Site in a Protein; 2.3.2 Deriving 3D-QSARs
2.3.3 Similarity Analysis of a Set of Related Molecules2.4 Concluding Remarks and Outlook; II Pharmacodynamics; 3 Protein Selectivity Studies Using GRID-MIFs; 3.1 Introduction; 3.2 GRID Calculations and Chemometric Analysis; 3.2.1 Source and Selection of Target Structures; 3.2.2 Selection and Superimposition of Binding Sites; 3.2.3 Calculation of the Molecular Interaction Field; 3.2.4 Matrix Generation and Pretreatments; 3.2.4.1 Region Cut-outs; 3.2.5 GRID/PCA; 3.2.5.1 Score Plots; 3.2.5.2 Two-Dimensional Loading Plots; 3.2.5.3 Loading Contour Maps; 3.2.5.4 Problems of GRID/PCA
3.2.6 GRID/CPCA3.2.6.1 Block Unscaled Weights; 3.2.6.2 CPCA; 3.2.6.3 Identification of Important Variable Blocks for Selectivity; 3.2.6.4 Contour Plots; 3.3 Applications; 3.3.1 DNA Minor Groove Binding - Compare AAA and GGG Double Helix; 3.3.2 Dihydrofolate Reductase; 3.3.3 Cyclooxygenase; 3.3.4 Penicillin Acylase; 3.3.5 Serine Proteases; 3.3.5.1 S1 Pocket; 3.3.5.2 P Pocket; 3.3.5.3 D Pocket; 3.3.6 CYP450; 3.3.7 Target Family Landscapes of Protein Kinases; 3.3.8 Matrix Metalloproteinases (MMPs); 3.3.9 Nitric Oxide Synthases; 3.3.10 PPARs; 3.3.11 Bile Acid Transportation System
3.3.12 Ephrin Ligands and Eph Kinases3.4 Discussion and Conclusion; 4 FLAP: 4-Point Pharmacophore Fingerprints from GRID; 4.1 Introduction; 4.1.1 Pharmacophores and Pharmacophore Fingerprints; 4.1.2 FLAP; 4.2 FLAP Theory; 4.3 Docking; 4.3.1 GLUE: A New Docking Program Based on Pharmacophores; 4.3.2 Case Study; 4.4 Structure Based Virtual Screening (SBVS); 4.5 Ligand Based Virtual Screening (LBVS); 4.6 Protein Similarity; 4.7 TOPP (Triplets of Pharmacophoric Points); 4.8 Conclusions; 5 The Complexity of Molecular Interaction: Molecular Shape Fingerprints by the PathFinder Approach
5.1 Introduction
Sommario/riassunto: This unique reference source, edited by the world's most respected expert on molecular interaction field software, covers all relevant principles of the GRID force field and its applications in medicinal chemistry. Entire chapters on 3D-QSAR, pharmacophore searches, docking studies, metabolism predictions and protein selectivity studies, among others, offer a concise overview of this emerging field. As an added bonus, this handbook includes a CD-ROM with the latest commercial versions of the GRID program and related software.
Titolo autorizzato: Molecular Interaction Fields  Visualizza cluster
ISBN: 1-280-85421-9
9786610854219
3-527-60767-6
3-527-60713-7
Formato: Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione: Inglese
Record Nr.: 9910829869103321
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Serie: Methods and Principles in Medicinal Chemistry