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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1991-10-23
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pubmed:abstractText |
A series of fluorine and iodine analogues of clorgyline was synthesized and evaluated for inhibitory potency and selectivity toward monoamine oxidase A (MAO-A). Among them, N-[3-(2,4-dichloro-6-iodophenoxy)propyl]-N-methyl-2-propynylami ne (3d), N-[3-(4-chloro-2-fluorophenoxy)propyl]-N-methyl-2-propynylamine (3f) and N-[3-(2-chloro-4-fluorophenoxy)propyl]-N-methyl-2-propynylamine (3g) were found to have high inhibitory potency and selectivity toward MAO-A comparable to those of clorgyline itself. Thus, they were considered for advanced development as radiofluorinated and radioiodinated ligands that may be useful for functional MAO-A studies in the living brain with positron emission tomography and single photon emission computer tomography.
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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 |
Apr
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pubmed:issn |
0009-2363
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
39
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1038-40
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:1893487-Animals,
pubmed-meshheading:1893487-Brain,
pubmed-meshheading:1893487-Clorgyline,
pubmed-meshheading:1893487-Fluorine,
pubmed-meshheading:1893487-Iodine,
pubmed-meshheading:1893487-Monoamine Oxidase,
pubmed-meshheading:1893487-Rats,
pubmed-meshheading:1893487-Tomography, Emission-Computed
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pubmed:year |
1991
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pubmed:articleTitle |
Synthesis of fluorine and iodine analogues of clorgyline and selective inhibition of monoamine oxidase A.
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pubmed:affiliation |
Osaka University of Pharmaceutical Sciences, Japan.
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pubmed:publicationType |
Journal Article
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