A convenient synthesis of 2-amino-2-oxazolines and their pharmacological evaluation at cloned human α adrenergic receptors

A convenient synthesis of 2-amino-2-oxazolines and their pharmacological evaluation at cloned human α adrenergic receptors New imidazoline/α2-adrenoceptors affecting compounds—4(5)-(2-aminoethyl)imidazoline (dihydrohistamine) derivatives. Synthesis and receptor affinity studies Synthesis and biological activities of 2-[(heteroaryl)methyl]imidazolines Radioiodinated p-iodoclonidine. A high-affinity probe for the .alpha.2-adrenergic receptor Heteroaromatic analogs of the .alpha.2-adrenoreceptor partial agonist clonidine Pyridinylpiperazines, a new class of selective .alpha.2-adrenoceptor antagonists .alpha.-Adrenoceptor reagents. 2. Effects of modification of the 1,4-benzodioxan ring system on .alpha.-adrenoreceptor activity Guanidine and 2-Aminoimidazoline Aromatic Derivatives as α₂-Adrenoceptor Ligands: Searching for Structure−Activity Relationships Synthesis and Evaluation of 2-[(5-Methylbenz-1-ox-4-azin-6-yl)imino]imidazoline, a Potent, Peripherally Acting α₂Adrenoceptor Agonist Novel synthesis and pharmacological evaluation as α2-adrenoceptor ligands of O-phenylisouronium salts