Recognition in molecularly imprinted polymer α2-adrenoreceptor mimics

Recognition in molecularly imprinted polymer α2-adrenoreceptor mimics Yohimbine dimers exhibiting binding selectivities for human α 2a - versus α 2b -adrenergic receptors Affinity of 2-(tetrahydroisoquinolin-2-ylmethyl)- and 2-(isoindolin-2-ylmethyl)imidazolines for .alpha.-adrenoceptors. Differential affinity of imidazolines for the [3H]idazoxan-labeled .alpha.2-adrenoceptor vs the [3H]yohimbine-labeled site Synthesis and biological studies of yohimbine derivatives on human α2C-adrenergic receptors α₂-Adrenoreceptors Profile Modulation. 3. (R)-(+)-m-Nitrobiphenyline, a New Efficient and α_2C-Subtype Selective Agonist Methylation of imidazoline related compounds leads to loss of α2-adrenoceptor affinity. Synthesis and biological evaluation of selective I1 imidazoline receptor ligands Structure-affinity relationships of 12-sulfonyl derivatives of 5,8,8a,9,10,11,12,12a,13,13a-decahydro-6H-isoquino[2,1-g][1,6]naphthyridines at .alpha.-adrenoceptors α₂-Adrenoreceptors Profile Modulation. 2. Biphenyline Analogues as Tools for Selective Activation of the α_2C-Subtype Conformationally defined adrenergic agents. 1. Design and synthesis of novel .alpha.2-selective adrenergic agents: electrostatic repulsion based conformational prototypes Design and synthesis of selective α1B adrenoceptor antagonists