Pharmacological Characterization of a Novel α2C-Adrenoceptor AgonistN-[3,4-dihydro-4-(1H-imidazol-4-ylmethyl)-2H-1, 4-benzoxazin-6-yl]-N-ethyl-N′-methylurea (Compound A)

Author:

Corboz Michel R.,Rivelli Maria A.,McCormick Kevin D.,Wan Yuntao,Shah Himanshu,Umland Shelby,Lieber Gisela,Jia Yanlin,McLeod Robbie L.,Morgan Cynthia,Varty Geoffrey B.,Wu Jie,Feng Kung-I,Boyce Christopher W.,Aslanian Robert G.,Palamanda Jai,Nomeir Amin A.,Korfmacher Walter,Hunter John C.,Anthes John C.,Hey John A.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference45 articles.

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3. Characterization of the α2C adrenergic receptor subtype in the opossum kidney and in the OK cell line;Blaxall;J Pharmacol Exp Ther,1991

4. Feedback Inhibition of Catecholamine Release by Two Different α 2 -Adrenoceptor Subtypes Prevents Progression of Heart Failure

5. International Union of Pharmacology nomenclature of adrenoceptors;Bylund;Pharmacol Rev,1994

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