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Molecular Recognition in Pharmacology
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Molecular Recognition in Pharmacology

Book Details

Format Paperback / Softback
ISBN-10 1032432942
ISBN-13 9781032432946
Publisher Taylor & Francis Ltd
Imprint CRC Press
Country of Manufacture GB
Country of Publication GB
Publication Date May 5th, 2025
Print length 188 Pages
Weight 380 grams
Ksh 9,350.00
Werezi Extended Catalogue 0 in stock

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This unique volume gives the basics of thermodynamics and kinetics of complex formation between ligands and receptors. The book is intended for pharmacologists, chemists, physics engaged in the creation of new medicinal substances.

This unique volume traces the behavior of the drug substance, starting from the initial pre-contact stage, and ending with the formation of the complex. Molecular recognition lies in the foundation of every life form and includes many mysteries. Currently, studies on this topic in pharmacology are limited to determining the properties of complexes of medicinal substances (drugs) with specific (complementary) biomolecules: receptors, enzymes, ion channels etc. The results present the mechanisms preventing drugs from such non-specific binding. This direction is very fruitful, although the phenomenon of molecular recognition is far wider.

Features

  • Presents the basics of thermodynamics and kinetics of complex formation between ligands and receptors
  • Selected novel therapeutic concepts are tested and validated
  • Provides a review of the pharmacophore approach and drug design methods
  • By its nature, pharmacology is a multi-disciplinary science, hence, disciplinary areas include chemistry, biology and neuroscience
  • Discusses hot topics including 3D structure determination techniques and in silico methods and neural networks

The main theme of the book is the consideration of mechanisms created by nature to protect physiologically active substances from being stuck on nonspecific acceptors in the body. The book describes the materials that aid in the development of new medicinal substances. It is intended for researchers, as well as upper-level undergraduate and graduate students interested in the problems of molecular pharmacology and drug design.


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