Source:http://linkedlifedata.com/resource/pubmed/id/16843672
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
21
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pubmed:dateCreated |
2006-9-25
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pubmed:abstractText |
A series of novel 2,4-diaminopyrimido[4,5-b]indol-6-ols has been synthesized and the in vitro cytotoxic activities were evaluated against four human cancer cell lines originating from solid tumors. An increase in activity was observed when a heteroaromatic ring was annulated on side g of the pyrimido[4,5-b]indole system to give compounds with activities comparable to ellipticine and cisplatin. To understand the experimental cytotoxic activities, QSAR investigations were performed, which showed a very good linearity between the experimental and predicted IC(50).
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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 |
Nov
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pubmed:issn |
0968-0896
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7282-92
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pubmed:meshHeading |
pubmed-meshheading:16843672-Antineoplastic Agents,
pubmed-meshheading:16843672-Magnetic Resonance Spectroscopy,
pubmed-meshheading:16843672-Mass Spectrometry,
pubmed-meshheading:16843672-Pyrimidines,
pubmed-meshheading:16843672-Quantitative Structure-Activity Relationship,
pubmed-meshheading:16843672-Spectrophotometry, Infrared
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pubmed:year |
2006
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pubmed:articleTitle |
2,4-Diamino-9H-pyrimido[4,5-b]indol-5-ols: synthesis, in vitro cytotoxic activity, and QSAR investigations.
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pubmed:affiliation |
Institut für Pharmazie und Lebensmittelchemie, Emil Fischer Centrum, Friedrich-Alexander-Universität, Schuhstr. 19, D-91052 Erlangen, Germany.
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pubmed:publicationType |
Journal Article
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