Molecular characterization of pharmacological properties of T-0509 for β-adrenoceptors

Author:

Sato Yoji,Kurose Hitoshi,Isogaya Masafumi,Nagao Taku

Publisher

Elsevier BV

Subject

Pharmacology

Reference20 articles.

1. Use of eukaryotic expression technology in the functional analysis of a cloned genes;Cullen,1987

2. A temary complex model explains the agonist-specific binding properties of the adenylate cyclase-coupled β-adrenergic receptor;DeLean;J. Biol. Chem.,1982

3. β1- and β2-adrenergic receptors display subtype-selective coupling to Gs;Green;Mol. Pharmacol.,1992

4. Effects of four diltiazem stereoisomers on binding of d-cis-[3H]diltiazem and (+)-[3H]PN200-110 to rabbit T-tuble calcium channels;Ikeda;Eur. J. Pharmacol. Mol. Pharmacol. Sect.,1991

5. In Kitten ventricular myocardium, the inotropic potency of an agonist is determined by both its intrinsic activity for the adenylyl cyclase and its affinity for the β-adrenoceptors;Kaumann;Naunyn-Schmiedeberg's Arch. Pharmacol.,1981

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