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

• Autore: Cruciani Gabriele
• 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
• 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
• Serie: Methods and Principles in Medicinal Chemistry