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Volumn 38, Issue 5, 1986, Pages 374-379

Characterization of flufylline, fluprofylline, ritanserin, butanserin and R 56413 with respect to in‐vivo α1‐, α2‐ and 5‐HT2‐receptor antagonism and in‐vitro affinity for α1‐, α2‐ and 5‐HT2‐receptors: comparison with ketanserin

(8) Korstanje, C a Sprenkels, R a Doods, H N a Hugtenburg, J G a Boddeke, E a Batink, H D a Thoolen, M J M C a Van Zwieten, P A a

a UNIVERSITY OF AMSTERDAM (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA 1 ADRENERGIC RECEPTOR; ALPHA 2 ADRENERGIC RECEPTOR; BUTANSERIN; FLUFYLLINE; FLUPROFYLLINE; KETANSERIN; MIANSERIN; MIANSERIN H 3; PRAZOSIN; PRAZOSIN H 3; RADIOISOTOPE; RITANSERIN; SEGANSERIN; SEROTONIN 2 RECEPTOR; SGD 144/80; SGD 195/78; UNCLASSIFIED DRUG; YOHIMBINE; YOHIMBINE H 3;

ANIMAL EXPERIMENT; ARTICLE; CENTRAL NERVOUS SYSTEM; DRUG COMPARISON; DRUG INTERACTION; DRUG RECEPTOR BINDING; INTRAVENOUS DRUG ADMINISTRATION; NONHUMAN; PHARMACOKINETICS; PRIORITY JOURNAL; RAT;

ADRENERGIC ALPHA-ANTAGONISTS; ANIMALS; BINDING, COMPETITIVE; BLOOD PRESSURE; BRAIN; DECEREBRATE STATE; HISTAMINE H2 ANTAGONISTS; KETANSERIN; MALE; PIPERIDINES; RATS; RATS, INBRED STRAINS; RITANSERIN; SEROTONIN ANTAGONISTS; THEOPHYLLINE; VASOCONSTRICTION;

EID: 0022576736 PISSN: 00223573 EISSN: 20427158 Source Type: Journal
DOI: 10.1111/j.2042-7158.1986.tb04590.x Document Type: Article

Times cited : (19)

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