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Neurochem Int ; 51(5): 268-76, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17643557

ABSTRACT

Three-dimensional structure-activity relationship studies of alpha2a-adrenoceptor agonists were carried out by Distance Comparison (DISCOthech) and Comparative Molecular Field Analysis (CoMFA) methods to define the pharmacophore and a quantitative model, respectively, of this class of compounds. The statistical validation of the CoMFA model indicates its high predictive performance for binding affinities of new alpha2a-adrenoceptor agonists.


Subject(s)
Adrenergic alpha-2 Receptor Agonists , Adrenergic alpha-Agonists/chemistry , Adrenergic alpha-Agonists/pharmacology , Receptors, Adrenergic, alpha-2/chemistry , Algorithms , Ligands , Models, Molecular , Molecular Conformation , Quantitative Structure-Activity Relationship , Reproducibility of Results
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