Source:http://linkedlifedata.com/resource/pubmed/id/10399841
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1999-9-27
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pubmed:abstractText |
Benzo[c]phenanthridine skeleton was synthesized from easily available starting N-methyl-o-toluamide 2 and o-methylbenzonitrile 5 in 7 steps. Radical cyclization of styrene 10 afforded 6,11-dimethyl-6,11-dihydro-5H-indeno[1,2-c]isoquinolin-5-one 13. Most 3-arylisoquinolines have displayed strong activities against human tumor cell lines. Especially, indenoisoquinolinone 13 exhibited excellent cytotoxicity (IC50 = 0.002 microgram/ml; HCT 15).
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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 |
Jun
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pubmed:issn |
0009-2363
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
47
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
900-2
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10399841-Antineoplastic Agents,
pubmed-meshheading:10399841-Cell Survival,
pubmed-meshheading:10399841-Drug Screening Assays, Antitumor,
pubmed-meshheading:10399841-Humans,
pubmed-meshheading:10399841-Isoquinolines,
pubmed-meshheading:10399841-Phenanthridines,
pubmed-meshheading:10399841-Tumor Cells, Cultured
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pubmed:year |
1999
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pubmed:articleTitle |
A novel synthesis of benzo[c]phenanthridine skeleton and biological evaluation of isoquinoline derivatives.
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pubmed:affiliation |
College of Pharmacy, Chonnam National University, Kwangju, Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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