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Volumn 353, Issue 3, 1996, Pages 290-294
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The moderate affinity of clozapine at H3 receptors is not shared by its two major metabolites and by structurally related and unrelated atypical neuroleptics
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Author keywords
3H N( ) methylhistamine binding; Atypical neuroleptics; Clozapine; Clozapine N oxide; H3 receptors; N Desmethylclozapine; Olanzapine; Risperidone
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Indexed keywords
ALPHA METHYLHISTAMINE;
CLOZAPINE;
CLOZAPINE N OXIDE;
DESIPRAMINE;
DRUG METABOLITE;
HISTAMINE;
HISTAMINE H3 RECEPTOR;
N METHYLHISTAMINE;
NEUROLEPTIC AGENT;
NORADRENALIN;
NORCLOZAPINE;
OLANZAPINE;
RADIOLIGAND;
RAUWOLSCINE;
REMOXIPRIDE;
RISPERIDONE;
THIORIDAZINE;
UNCLASSIFIED DRUG;
ZOTEPINE;
ANIMAL TISSUE;
ARTICLE;
BRAIN CORTEX;
BRAIN HOMOGENATE;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG ANTAGONISM;
ELECTROSTIMULATION;
LIGAND BINDING;
MALE;
NONHUMAN;
NORADRENALIN RELEASE;
RAT;
RECEPTOR AFFINITY;
ANIMALS;
ANTIPSYCHOTIC AGENTS;
BENZODIAZEPINES;
BINDING, COMPETITIVE;
CLOZAPINE;
DIBENZOTHIEPINS;
DOSE-RESPONSE RELATIONSHIP, DRUG;
HISTAMINE ANTAGONISTS;
ISOTOPE LABELING;
MALE;
METHYLHISTAMINES;
MICE;
PIRENZEPINE;
RATS;
RATS, WISTAR;
RECEPTORS, HISTAMINE H3;
REMOXIPRIDE;
RISPERIDONE;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIORIDAZINE;
TRITIUM;
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EID: 0029990288
PISSN: 00281298
EISSN: None
Source Type: Journal
DOI: 10.1007/BF00168630 Document Type: Article |
Times cited : (28)
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References (17)
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