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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
|
pubmed:dateCreated |
1990-12-6
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pubmed:abstractText |
4-(2-Methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazole (5) is a highly potent member of a structurally novel series of selective serotonin-3 receptor antagonists. The synthesis of tritiated 5 and its binding profile in neuroblastoma-glioma 108-15 cells are described. Furthermore, in vivo studies in rat with this radioligand indicate that it effectively penetrates the blood-brain barrier upon peripheral administration. Thus, 5 should be a useful pharmacological tool for both in vitro and in vivo studies of this class of compounds.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
33
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
N
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pubmed:pagination |
3020-3
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:2231600-Animals,
pubmed-meshheading:2231600-Blood-Brain Barrier,
pubmed-meshheading:2231600-Brain,
pubmed-meshheading:2231600-Chemical Phenomena,
pubmed-meshheading:2231600-Chemistry,
pubmed-meshheading:2231600-Glioma,
pubmed-meshheading:2231600-Imidazoles,
pubmed-meshheading:2231600-Mice,
pubmed-meshheading:2231600-Molecular Structure,
pubmed-meshheading:2231600-Neuroblastoma,
pubmed-meshheading:2231600-Serotonin Antagonists,
pubmed-meshheading:2231600-Thiazoles,
pubmed-meshheading:2231600-Tumor Cells, Cultured
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pubmed:year |
1990
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pubmed:articleTitle |
Synthesis, in vitro binding profile, and central nervous system penetrability of the highly potent 5-HT3 receptor antagonist [3H]-4-(2-methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazole.
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pubmed:affiliation |
Pfizer Central Research, Department of Medicinal Chemistry, Groton, Connecticut 06340.
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pubmed:publicationType |
Journal Article
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