Source:http://linkedlifedata.com/resource/pubmed/id/12643915
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2003-3-19
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pubmed:abstractText |
Three novel 4-deacetoxy-1,7-dideoxy azetidine paclitaxel analogues were synthesized through a convenient route that employed hydroboration-amination and intramolecular S(N)2-type substitution reaction from a natural taxoid taxinine. All analogues have been tested for cytotoxicity against three human tumor cell lines. None of them showed remarkable cytotoxicity compared to paclitaxel against tested tumor cell lines.
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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 |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
24
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1075-7
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:12643915-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:12643915-Azetidines,
pubmed-meshheading:12643915-Drug Screening Assays, Antitumor,
pubmed-meshheading:12643915-Humans,
pubmed-meshheading:12643915-Indicators and Reagents,
pubmed-meshheading:12643915-Paclitaxel,
pubmed-meshheading:12643915-Structure-Activity Relationship,
pubmed-meshheading:12643915-Tumor Cells, Cultured
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pubmed:year |
2003
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pubmed:articleTitle |
Synthesis and biological evaluation of 4-deacetoxy-1,7-dideoxy azetidine paclitaxel analogues.
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pubmed:affiliation |
Laboratory of Applied Bioorganic Chemistry, Division of Life Science, Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori-Amamiyamachi, Aoba-ku, Sendai 981-8555, Japan.
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pubmed:publicationType |
Journal Article
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