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TitleQSAR and drug design [electronic resource] : new developments and applications / edited by Toshio Fujita
Imprint Amsterdam ; New York : Elsevier, 1995
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Descript xiv, 493 p. : ill. (some col.) ; 25 cm


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.<P>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.<P>A variety of methodologies and procedures are presented in this single volume, along with their methodological philosophies

Drugs -- Structure-activity relationships -- Congresses QSAR (Biochemistry) -- Congresses Drugs -- Design -- Congresses Structure-Activity Relationship -- Congresses Drug Design -- Congresses Electronic books.


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