Interaction of d-tubocurarine analogs with mutant 5-HT3 receptors

Neuropharmacology

Volumn 43, Issue 3, 2002, Pages 367-373

  Yan, Dong ^a   White, Michael M ^a  

^a DREXEL UNIVERSITY COLLEGE OF MEDICINE   (United States)

Author keywords

5 HT; 5 HT3 receptor; d tubocurarine analogs; Mutagenesis

Indexed keywords

12' O METHYLCHONDOCURARINE; 7' O METHYLCHONDOCURARINE; BROMO DEXTRO TUBOCURARINE; CHONDOCURARINE; CHONDROCURINE; DIMETHYLTUBOCURARINE CHLORIDE; IODO DEXTRO TUBOCURARINE; O,O DIMETHYLTUBOCURINE; SEROTONIN 3 ANTAGONIST; SEROTONIN 3 RECEPTOR; SULFO DEXTRO TUBOCURARINE; TUBOCURARINE CHLORIDE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING AFFINITY; BINDING SITE; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG RECEPTOR BINDING; IC 50; LIGAND BINDING; MOUSE; MUTATION; NONHUMAN; PRIORITY JOURNAL; WILD TYPE;

ALGORITHMS; CLONING, MOLECULAR; DNA, COMPLEMENTARY; HUMANS; LIGANDS; MUTATION; NEUROMUSCULAR NONDEPOLARIZING AGENTS; RECEPTORS, SEROTONIN; RECEPTORS, SEROTONIN, 5-HT3; SEROTONIN ANTAGONISTS; TRANSFECTION; TUBOCURARINE; TUMOR CELLS, CULTURED;

EID: 0036710144     PISSN: 00283908     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0028-3908(02)00125-9     Document Type: Article

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