Source:http://linkedlifedata.com/resource/pubmed/id/10234736
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1999-6-28
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pubmed:abstractText |
A novel series of 3-(3-phenyl-isoxazol-5-yl) or 3-[(3-phenyl-isoxazol-5-yl)amino] substituted 4(3H)-quinazolinone derivatives was synthesized. The compounds were tested for their antineoplastic activity in vitro against Raji (human Burkitt limphoma). K-562 (human chronic myelogeneous leukemia) and U937 (human histiocytic limphoma) cell lines. The most active quinazolinones showed IC50 values in the range 16-30 microM.
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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 |
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 |
251-4
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pubmed:dateRevised |
2007-1-29
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pubmed:meshHeading |
pubmed-meshheading:10234736-Antineoplastic Agents,
pubmed-meshheading:10234736-Drug Screening Assays, Antitumor,
pubmed-meshheading:10234736-Humans,
pubmed-meshheading:10234736-Inhibitory Concentration 50,
pubmed-meshheading:10234736-Isoxazoles,
pubmed-meshheading:10234736-Magnetic Resonance Spectroscopy,
pubmed-meshheading:10234736-Quinazolines,
pubmed-meshheading:10234736-Spectrophotometry, Infrared,
pubmed-meshheading:10234736-Tumor Cells, Cultured
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pubmed:year |
1999
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pubmed:articleTitle |
Synthesis of new 3-(3-phenyl-isoxazol-5-yl) or 3-[(3-phenyl-isoxazol-5-yl)-amino] substituted 4(3H)-quinazolinone derivatives with antineoplastic activity.
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pubmed:affiliation |
Dipartimento di Chimica e Tecnologie Farmaceutiche, Università degli Studi di Palermo, Italy.
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pubmed:publicationType |
Journal Article
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