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Bioorg Med Chem Lett. 2004 Apr 19;14(8):1845-8.

Pharmacology of the agonist binding sites of rat neuronal nicotinic receptor subtypes expressed in HEK 293 cells.

Author information

1
Department of Pharmacology, Georgetown University School of Medicine, Washington, DC 20057, USA.

Abstract

The binding affinities of agonists at heteromeric nicotinic receptors composed of rat alpha2, alpha3 and alpha4 subunits in combination with beta2 or beta4 subunits were examined in stably transfected HEK 293 cells. In most cases, the affinities of agonists were higher at receptors composed of an alpha subunit in combination with the beta2 subunit than the beta4 subunit, and in some cases this difference was quite large (>250 times), suggesting the possibility of developing subtype-selective ligands and therapeutically useful drugs.

PMID:
15050613
DOI:
10.1016/j.bmcl.2003.09.105
[Indexed for MEDLINE]

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