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Rational Drug Design

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Cover of 'Rational Drug Design'

Table of Contents

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    Book Overview
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    Chapter 1 Molecular Dynamics Simulations on the Bioactive Molecule of hIAPP22–29 (NFGAILSS) and Rational Drug Design
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    Chapter 2 Development of Peptide-Based Inhibitors of Amylin Aggregation Employing Aromatic and Electrostatic Repulsion
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    Chapter 3 In Silico Drug Design: Non-peptide Mimetics for the Immunotherapy of Multiple Sclerosis
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    Chapter 4 Binding Moiety Mapping by Saturation Transfer Difference NMR
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    Chapter 5 Protein-Ligand Docking in Drug Design: Performance Assessment and Binding-Pose Selection
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    Chapter 6 Rational Drug Design Using Integrative Structural Biology
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    Chapter 7 Enalos+ KNIME Nodes: New Cheminformatics Tools for Drug Discovery
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    Chapter 8 Bioguided Design of Trypanosomicidal Compounds: A Successful Strategy in Drug Discovery
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    Chapter 9 A Hybrid Virtual Screening Protocol Based on Binding Mode Similarity
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    Chapter 10 Single Step Determination of Unlabeled Compound Kinetics Using a Competition Association Binding Method Employing Time-Resolved FRET
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    Chapter 11 Dynamic Undocking: A Novel Method for Structure-Based Drug Discovery
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    Chapter 12 The Impact of Lipophilicity in Drug Discovery: Rapid Measurements by Means of Reversed-Phase HPLC
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    Chapter 13 Exploring Polypharmacology in Drug Design
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    Chapter 14 Development of Nuclear Receptor Modulators
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    Chapter 15 In Silico Screening of Compound Libraries Using a Consensus of Orthogonal Methodologies
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    Chapter 16 Insights in Organometallic Synthesis of Various Adamantane Derivatives with Sigma Receptor-Binding Affinity and Antiproliferative/Anticancer Activity
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    Chapter 17 Supervised Molecular Dynamics (SuMD) Approaches in Drug Design
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    Chapter 18 Lead Identification Through the Synergistic Action of Biomolecular NMR and In Silico Methodologies
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    Chapter 19 The Use of Dynamic Pharmacophore in Computer-Aided Hit Discovery: A Case Study
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    Chapter 20 Rational Development of MAGL Inhibitors
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    Chapter 21 Application of Virtual Screening Approaches for the Identification of Small Molecule Inhibitors of the Methyllysine Reader Protein Spindlin1
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    Chapter 22 Designing Natural Product Hybrids Bearing Triple Antiplatelet Profile and Evaluating Their Human Plasma Stability
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    Chapter 23 Pharmacophore Generation and 3D-QSAR Model Development Using PHASE
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    Chapter 24 Design of Drugs by Filtering Through ADMET, Physicochemical and Ligand-Target Flexibility Properties
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    Chapter 25 Reactions in NMR Tubes as Key Weapon in Rational Drug Design
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    Chapter 26 Application of Multiscale Simulation Tools on GPCRs. An Example with Angiotensin II Type 1 Receptor
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    Chapter 27 Angiotensin II Type 1 Receptor Homology Models: A Comparison Between In Silico and the Crystal Structures
Attention for Chapter 6: Rational Drug Design Using Integrative Structural Biology
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Chapter title
Rational Drug Design Using Integrative Structural Biology
Chapter number 6
Book title
Rational Drug Design
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-8630-9_6
Pubmed ID
Book ISBNs
978-1-4939-8629-3, 978-1-4939-8630-9
Authors

Magda S. Chegkazi, Michael Mamais, Anastasia I. Sotiropoulou, Evangelia D. Chrysina, Chegkazi, Magda S., Mamais, Michael, Sotiropoulou, Anastasia I., Chrysina, Evangelia D.

Abstract

Modern drug discovery and design approaches rely heavily on high-throughput methods and state-of-the-art infrastructures with robotic facilities and sophisticated platforms. However, the anticipated research output that would eventually lead to new drugs with minimal or no side effects to the market has not been achieved. Despite the vast amount of information generated, very little is converted to knowledge and even less is capitalized for cross-discipline research actions. Therefore, the need for re-launching rational approaches has become apparent. Here we present an overview of the new trends in rational drug design using integrative structural biology with emphasis on X-ray protein crystallography and small molecules as ligands. With the aim to increase researchers' awareness on the available possibilities to perform front line research, we also underline the benefits and enhanced prospects offered to the scientific community, through access to research infrastructures.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 26 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 26 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 5 19%
Researcher 4 15%
Student > Ph. D. Student 3 12%
Professor 1 4%
Lecturer 1 4%
Other 1 4%
Unknown 11 42%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 15%
Chemistry 2 8%
Nursing and Health Professions 1 4%
Computer Science 1 4%
Agricultural and Biological Sciences 1 4%
Other 2 8%
Unknown 15 58%