Source:http://linkedlifedata.com/resource/pubmed/id/11462978
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2001-7-20
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pubmed:abstractText |
A great need exists for antipsychotic drugs which will not induce extrapyramidal symptoms (EPS) and tardive dyskinesias (TDs). These side effects are deemed to be a consequence of nonselective blockade of nigrostriatal and mesolimbic dopamine D2 receptors. Nondyskinetic clozapine (1) is a low-potency D2 dopamine receptor antagonist which appears to act selectively in the mesolimbic area. In this work dopamine antagonism was assessed in two mouse behavioral assays: antagonism of apomorphine-induced climbing and antagonism of apomorphine-induced disruption of swimming. The potential for the liability of dyskinesias was determined in haloperidol-sensitized Cebus monkeys. Initial examination of a few close cogeners of 1 enhanced confidence in the Cebus model as a predictor of dyskinetic potential. Considering dibenzazepines, 2 was not dyskinetic whereas 2a was dyskinetic. Among dibenzodiazepines, 1 did not induce dyskinesias whereas its N-2-(2-hydroxyethoxy)ethyl analogue 3 was dyskinetic. The emergence of such distinctions presented an opportunity. Thus, aromatic and N-substituted analogues of 6-(piperazin-1-yl)-11H-dibenz[b,e]azepines and 11-(piperazin-1-yl)dibenzo[b,f][1,4]thiazepines and -oxazepines were prepared and evaluated. 11-(4-[2-(2-Hydroxyethoxy)ethyl]piperazin-1-yl)dibenzo[b,f][1,4]thiazepine (23) was found to be an apomorphine antagonist comparable to clozapine. It was essentially nondyskinetic in the Cebus model. With 23 as a platform, a number of N-substituted analogues were found to be good apomorphine antagonists but all were dyskinetic.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antipsychotic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Apomorphine,
http://linkedlifedata.com/resource/pubmed/chemical/Dibenzothiazepines,
http://linkedlifedata.com/resource/pubmed/chemical/Dopamine Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D2,
http://linkedlifedata.com/resource/pubmed/chemical/quetiapine
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
44
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
372-89
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pubmed:dateRevised |
2004-4-5
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pubmed:meshHeading |
pubmed-meshheading:11462978-Animals,
pubmed-meshheading:11462978-Antipsychotic Agents,
pubmed-meshheading:11462978-Apomorphine,
pubmed-meshheading:11462978-Behavior, Animal,
pubmed-meshheading:11462978-Cebus,
pubmed-meshheading:11462978-Dibenzothiazepines,
pubmed-meshheading:11462978-Dopamine Antagonists,
pubmed-meshheading:11462978-Dyskinesia, Drug-Induced,
pubmed-meshheading:11462978-Female,
pubmed-meshheading:11462978-Male,
pubmed-meshheading:11462978-Mice,
pubmed-meshheading:11462978-Receptors, Dopamine D2,
pubmed-meshheading:11462978-Stereoisomerism,
pubmed-meshheading:11462978-Structure-Activity Relationship
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pubmed:year |
2001
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pubmed:articleTitle |
Behavioral approach to nondyskinetic dopamine antagonists: identification of seroquel.
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pubmed:affiliation |
Department of Medicinal Chemistry, AstraZeneca Pharmaceuticals LP, Wilmington, Delaware 19850-5437, USA. kcassoc@inet.net
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pubmed:publicationType |
Journal Article
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