Source:http://linkedlifedata.com/resource/pubmed/id/10192109
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1999-6-1
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pubmed:abstractText |
Some naphtho[1,2-b]furan, furo[2,3-f], furo[2,3-g] and furo[3,2-g]quinoline derivatives have been submitted to in vitro cytotoxic tests towards L 1210, MDA-MB 231 and PC3 cell lines. Among them, the furoquinone structures exhibited the most interesting IC50 values.
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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 |
Mar
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pubmed:issn |
0031-7144
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
54
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
215-8
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pubmed:dateRevised |
2007-1-29
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pubmed:meshHeading |
pubmed-meshheading:10192109-Antineoplastic Agents,
pubmed-meshheading:10192109-Drug Screening Assays, Antitumor,
pubmed-meshheading:10192109-Furans,
pubmed-meshheading:10192109-Humans,
pubmed-meshheading:10192109-Naphthalenes,
pubmed-meshheading:10192109-Quinolones,
pubmed-meshheading:10192109-Tumor Cells, Cultured
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pubmed:year |
1999
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pubmed:articleTitle |
In vitro cytotoxic activity of naphtho[1,2-b]furan, furo[2,3-f], furo[2,3-g] and furo[3,2-g]quinoline derivatives.
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pubmed:affiliation |
Laboratoire de Chimie Organique, Institut des Sciences Pharmaceutiques et Biologiques, Lyon, France.
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pubmed:publicationType |
Journal Article
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