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Chemical drug design / edited by Girish Kumar Gupta, Vinod Kumar. — 1 online resource (xii, 285 pages .). — In English. — <URL:http://elib.fa.ru/ebsco/1385590.pdf>.

Дата создания записи: 09.12.2016

Тематика: Drugs — Design.; Pharmaceutical chemistry.; Drug Design.; MEDICAL — Pharmacology.; Drugs — Design.; Pharmaceutical chemistry.; Wirkstoffdesign.

Коллекции: EBSCO

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Аннотация

Chemical Drug Design provides a compact overview on recent advances in this rapidly developing field. With contributions on in silico drug design, natural product based compounds, as well as on ligand- and structure-based approaches, the authors present innovative methods and techniques for identifying and synthetically designing novel drugs.

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Оглавление

  • Preface
  • Table of Contents
  • List of Contributing Authors
  • 1 Overview of chemical drug design
    • 1.1 Drug design
    • 1.2 Rational drug design
    • 1.3 Ligand-based drug design
    • 1.4 Structure-based drug design
    • 1.5 Pharmacophore-based approaches
    • 1.6 Structure-based approaches
    • 1.7 New lead generation
    • 1.8 Structure evaluation
    • 1.9 Future directions
  • 2 Drug designing in novel drug discovery: Trends, scope and relevance
    • 2.1 Introduction
    • 2.2 Drug designing
    • 2.3 Applications of SBDD
    • 2.4 Applications of LBDD
    • 2.5 Role of cheminformatics in drug discovery
    • 2.6 Conclusion
  • 3 Structure- and ligand-based approaches in drug designing
    • 3.1 Drug discovery
    • 3.2 Drug design
    • 3.3 Drug designing techniques
    • 3.4 Quantitative Structure-Activity Relationship (QSAR)
    • 3.5 Physicochemical parameters
    • 3.6 Biological parameters
    • 3.7 Statistical terms in QSAR
  • 4 Drug design applied to natural products against neglected diseases
    • 4.1 Natural products
    • 4.2 Medicinal chemistry
    • 4.3 Docking
    • 4.4 Neglected diseases
    • 4.5 Final considerations
  • 5 Natural product hybrid compounds as drug leads
    • 5.1 Introduction
    • 5.2 Naturally occurring hybrids/conjugates of natural products
    • 5.3 Synthetic hybrids of whole natural products
    • 5.4 Conclusion
  • 6 Drug metabolism
    • 6.1 Introduction
    • 6.2 Phase I Metabolic reactions
    • 6.3 Oxidative mechanisms
    • 6.4 Reductive reactions
    • 6.5 Hydrolytic reactions
    • 6.6 Phase II conjugation reactions
    • 6.7 Factors affecting drug metabolism
  • 7 Mistletoe lectin: A promising cancer therapeutic
    • 7.1 Introduction
    • 7.2 Anticancer potency of bacteria/plant lectins
    • 7.3 Anticancer potency of mistletoe and the underlying mechanisms
    • 7.4 Mistletoe lectins
    • 7.5 Future directions
    • 7.6 Concluding remarks
  • 8 Antipsychotics
    • 8.1 Introduction
    • 8.2 History
    • 8.3 Etiology of schizophrenia and related psychoses
    • 8.4 Potential mechanism of action of antipsychotics
    • 8.5 Structure-activity relationships and pharmacology of the drugs
    • 8.6 Research into future treatments for schizophrenia and related psychoses
  • 9 Chemometric analysis: A novel tool for herbal drug analysis and designing
    • 9.1 Introduction
    • 9.2 Experimental
    • 9.3 Data analysis and quality evaluation
    • 9.4 Results and discussion
    • 9.5 Conclusion
  • 10 Copper and its complexes: A pharmaceutical perspectives
    • 10.1 Introduction
    • 10.2 Source of dietetic copper
    • 10.3 Recommended concentration of copper for human diet
    • 10.4 Copper consumption and suggestions
    • 10.5 Mechanism of copper transport in humans
    • 10.6 Copper deficiency and symptoms
    • 10.7 Copper metabolism and major diseases
    • 10.8 Copper metabolism and hypothesized health problems
    • 10.9 Copper complexes as an emerging tool in pharmaceutical sciences
    • 10.10 Concluding remarks
  • 11 Thiazole: A privileged scaffold in drug discovery
    • 11.1 Introduction
    • 11.2 Synthetic routes for the construction of the thiazole ring
    • 11.3 Thiazole as privileged scaffold in synthetic drugs
    • 11.4 Ritonavir
    • 11.5 Nitazoxanide
    • 11.6 Sulfathiazole
    • 11.7 Thiabendazole
    • 11.8 Fatostatin
    • 11.9 Dasatinib
    • 11.10 Tiazofurin
    • 11.11 CYC116
    • 11.12 NCH-31
    • 11.13 TAK-715
    • 11.14 Meloxicam
    • 11.15 Nizatidine
    • 11.16 Famotidine
    • 11.17 Conclusion
  • Index

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