ABSTRACT

As a result of new statistical and mathematical approaches, improved visualization tools, and recognition by international regulatory groups, quantitative structure-activity relationships (QSARs) now play important roles in pharmacology for the design of new drugs as well as in toxicology and ecotoxicology for hazard identification and risk assessm

part |2 pages

Part I. Actual 3D Models

part |2 pages

Part II. Around the 3D Approaches

part |2 pages

Part III. Beyond 3D

chapter 9|26 pages

4D-QSARs

chapter 10|14 pages

Induced-Fit in 5D- and 6D-QSAR Models

part |2 pages

Part IV. Receptor-Related Models