Literature DB >> 8524985

D4 dopamine receptor binding affinity does not distinguish between typical and atypical antipsychotic drugs.

B L Roth1, S Tandra, L H Burgess, D R Sibley, H Y Meltzer.   

Abstract

The affinities of 13 atypical and 12 typical antipsychotic drugs for the cloned rat D4 dopamine receptor and the D4/D2 ratios were examined. Of the atypical antipsychotic drugs tested, only clozapine, risperidone, olanzapine, zotepine and tiospirone had affinities less than 20 nM. In fact, many atypical antipsychotic drugs had relatively low affinities for the cloned rat D4 receptor, with Ki values greater than 100 nM (Seroquel, fluperlapine, tenilapine, FG5803 and melperone). Additionally, several typical antipsychotic drugs had high affinities for the cloned rat D4 receptor, with Kis less than 20 nM (loxapine, chlorpromazine, fluphenazine, mesoridazine, thioridazine and trifluoroperazine). The ratios of D2/D4 affinities did not differentiate between these two types of antipsychotic drugs. Thus, D4 dopamine receptor affinity, used as a single measure, does not distinguish between the group of typical and atypical antipsychotic drugs analyzed.

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Year:  1995        PMID: 8524985     DOI: 10.1007/bf02311185

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  20 in total

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Journal:  J Pharmacol Exp Ther       Date:  1994-11       Impact factor: 4.030

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Authors:  H H Van Tol; J R Bunzow; H C Guan; R K Sunahara; P Seeman; H B Niznik; O Civelli
Journal:  Nature       Date:  1991-04-18       Impact factor: 49.962

7.  Dopamine D4 versus D2 receptor selectivity of dopamine receptor antagonists: possible therapeutic implications.

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8.  Binding of typical and atypical antipsychotic agents to transiently expressed 5-HT1C receptors.

Authors:  B L Roth; R D Ciaranello; H Y Meltzer
Journal:  J Pharmacol Exp Ther       Date:  1992-03       Impact factor: 4.030

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Journal:  J Pharmacol Exp Ther       Date:  1992-02       Impact factor: 4.030

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  22 in total

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6.  Synthesis of unnatural alkaloid scaffolds by exploiting plant polyketide synthase.

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7.  The dopamine D2 antagonist eticlopride accelerates extinction and delays reacquisition of food self-administration in rats.

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