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
TABLE OF CONTENTS
part |2 pages
Part I. Actual 3D Models
part |2 pages
Part II. Around the 3D Approaches
part |2 pages
Part III. Beyond 3D
part |2 pages
Part IV. Receptor-Related Models