An Analysis of the β2‐Adrenoceptor Selectivity in Three Series of β‐Adrenoceptor Agonists

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Abstract
The aim of the study was to analyse the β2‐adrenoceptor selectivity earlier found in two series of catecholamines and one series of resorcinolamines (Johanssonet al.1986). The affinity of the compounds was assessed in binding studies in preparations from the guinea‐pig left heart ventricle (β1‐adrenoceptors) and the soleus muscle (β2‐adrenoceptors) using3H‐CGP‐12177 as radioligand. Further, the activation of the adenylate cyclase by the compounds was studied in the same preparations. Selectivity quotients were obtained from both functional effects and from affinity and adenylate cyclase activating studies. There was a good correlation between the selectivity quotients obtained in these two ways. Tertiary butyl substitution on the amino nitrogen gave the highest β2‐adrenoceptor selectivity in both the catechol and resorcinol series. In comparison with their isopropyl substituted analogues the β2‐adrenoceptor selectivity of these compounds (KWD 2026 and terbutaline) was mainly due to a change in affinity for the β1‐ and β2‐adrenoceptors and, to a lesser degree, a change in intrinsic efficacy.