QSAR and drug design: new developments and applications
Gespeichert in:
Bibliographische Detailangaben
Format: Elektronisch E-Book
Sprache:English
Veröffentlicht: Amsterdam Elsevier 1995
Schriftenreihe:Pharmacochemistry library v. 23
Schlagworte:
Online-Zugang:Volltext
Beschreibung:"Based on topics presented at the annual Japanese (Quantitative) Structure-Activity Relationship Symposium and the biennial China-Japan Drug Design and Development Conference."
Based on topics presented at the Annual Japanese (Quantitative) Structure-Activity Relationship Symposium and the Biennial China-Japan Drug Design and Development conference, the topics in this volume cover almost every procedure and subdiscipline in the SAR discipline. They are categorized in three sections. Section one includes topics illustrating newer methodologies relating to ligand-receptor, molecular graphics and receptor modelling as well as the three-dimensional (Q)SAR examples with the active analogue approach and the comparative molecular field analysis. In section 2 the hydrophobicity parameters, log P (1-octanol/water) for compound series of medicinal-chemical interest are analysed physico-organic chemically. Section 3 contains the examples based on the traditional Hansch QSAR approach. A variety of methodologies and procedures are presented in this single volume, along with their methodological philosophies
Includes bibliographical references and index
Beschreibung:1 Online-Ressource (xiv, 493 p.)
ISBN:9780444886156
044488615X
9780080545004
0080545009

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