Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9743937 | Analytica Chimica Acta | 2005 | 4 Pages |
Abstract
For compounds G4, G5 and G6 the affinity (IC50) for β1-adrenergic binding sites was of the same magnitude of that from clenbuterol. By contrast, G8 showed a 100-fold higher affinity. On β2-adrenergic receptors the binding affinity was similar for G4 and G6, but about 10-fold higher for G5 and G8 with respect to that from clenbuterol.
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Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Cinzia Civitareale, Caterina Ambrosio, Maria Sbraccia, Maurizio Fiori, Gianfranco Brambilla, Cecilia Testa,