Source:http://linkedlifedata.com/resource/pubmed/id/16990003
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
23
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pubmed:dateCreated |
2006-11-10
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pubmed:abstractText |
Two novel dual functional agents, 3[3-(2,4-dinitro-phenylamino)-propyl]-5-fluoro-1H-pyrimidine-2,4-dione 7 and N-[3-(2,4-dinitro-phenylamino)-propoxy]urea 8, resulting from linkage of 2,4-dinitrophenylamine through three carbon atoms with 5-fluorouracil 5 and hydroxyurea 6, respectively, were prepared and their in vitro aerobic cytotoxicities in HT-29 cell line with and without radiation were determined. Compounds 7 and 8 unlike their components were not cytotoxic but showed radiosensitizing activity.
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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 |
Dec
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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 |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6034-8
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pubmed:meshHeading |
pubmed-meshheading:16990003-Aerobiosis,
pubmed-meshheading:16990003-Cell Survival,
pubmed-meshheading:16990003-Fluorouracil,
pubmed-meshheading:16990003-HT29 Cells,
pubmed-meshheading:16990003-Humans,
pubmed-meshheading:16990003-Hydroxyurea,
pubmed-meshheading:16990003-Molecular Structure,
pubmed-meshheading:16990003-Nitro Compounds,
pubmed-meshheading:16990003-Radiation-Sensitizing Agents,
pubmed-meshheading:16990003-Structure-Activity Relationship
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pubmed:year |
2006
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pubmed:articleTitle |
Synthesis, aerobic cytotoxicity, and radiosensitizing activity of novel 2,4-dinitrophenylamine tethered 5-fluorouracil and hydroxyurea.
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pubmed:affiliation |
Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran 14174, Iran. khalaj@ams.ac.ir <khalaj@ams.ac.ir>
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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