Zinc modulates antagonist interactions with D2-like dopamine receptors through distinct molecular mechanisms

Journal of Pharmacology and Experimental Therapeutics

Volumn 289, Issue 2, 1999, Pages 956-964

  Schetz, John A ^a   Chu, Alice ^a   Sibley, David R ^a  

^a NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 METHYLSPIPERONE; DOPAMINE 2 RECEPTOR; DOPAMINE 2 RECEPTOR BLOCKING AGENT; RACLOPRIDE; ZINC;

ALLOSTERISM; ANIMAL CELL; BINDING AFFINITY; CHO CELL; COMPETITIVE INHIBITION; CONFERENCE PAPER; DISSOCIATION CONSTANT; DOPAMINERGIC TRANSMISSION; DOSE RESPONSE; DRUG EFFECT; DRUG RECEPTOR BINDING; DRUG SELECTIVITY; ENTROPY; EQUILIBRIUM CONSTANT; MOLECULAR INTERACTION; NONHUMAN; PRIORITY JOURNAL; RECEPTOR OCCUPANCY;

ALGORITHMS; ANIMALS; CHO CELLS; CRICETINAE; CYCLIC AMP; DOPAMINE AGONISTS; DOPAMINE ANTAGONISTS; FORSKOLIN; KINETICS; RACLOPRIDE; RADIOLIGAND ASSAY; RECEPTORS, DOPAMINE D2; RECEPTORS, DOPAMINE D3; RECEPTORS, DOPAMINE D4; SALICYLAMIDES; SODIUM; SPIPERONE; THERMODYNAMICS; ZINC;

EID: 0032926451     PISSN: 00223565     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

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