Source:http://linkedlifedata.com/resource/pubmed/id/14611843
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
17
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pubmed:dateCreated |
2003-11-12
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pubmed:abstractText |
1-Methyl-1,2,3,4-tetrahydroisoquinoline (1MeTIQ) 1 and various 5- or 6,7-substituted analogues were synthesized and assayed for neurotoxicity towards SH-SY5Y cells. Among mono-substituted derivatives of 1, hydroxyl substitution decreased the toxicity, while methoxyl substitution increased it. Disubstituted derivatives of 1, 5a and 5b, showed the opposite tendency. Hydroxy-1MeTIQ derivatives were tested for neuroprotective activity, and 3b and 4b exhibited greater efficacy than 1. We suggest that hydroxy-1MeTIQ derivatives, especially 4b, may have potential for the treatment of Parkinson's disease.
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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 |
Sep
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2853-5
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:14611843-Cell Line, Tumor,
pubmed-meshheading:14611843-Cell Survival,
pubmed-meshheading:14611843-Dose-Response Relationship, Drug,
pubmed-meshheading:14611843-Humans,
pubmed-meshheading:14611843-Isoquinolines,
pubmed-meshheading:14611843-Neuroblastoma,
pubmed-meshheading:14611843-Neuroprotective Agents,
pubmed-meshheading:14611843-Structure-Activity Relationship,
pubmed-meshheading:14611843-Tetrahydroisoquinolines
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pubmed:year |
2003
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pubmed:articleTitle |
Neuroprotective or neurotoxic activity of 1-methyl-1,2,3,4-tetrahydroisoquinoline and related compounds.
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pubmed:affiliation |
Graduate School of Biomedical Sciences, Hiroshima University, Japan.
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pubmed:publicationType |
Journal Article
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