Source:http://linkedlifedata.com/resource/pubmed/id/12031338
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2002-5-28
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pubmed:abstractText |
Various 2-amido docetaxel analogues were prepared and evaluated for their cytotoxicities. Among them, m-methoxy and m-chlorobenzoylamido analogues were most active but not superior to docetaxel and paclitaxel, and D-seco analogues inactive. Change of 2-benzoate to 2-benzamide may not improve their activities to drug-resistant 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 |
Jun
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1543-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12031338-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:12031338-Drug Resistance, Neoplasm,
pubmed-meshheading:12031338-Inhibitory Concentration 50,
pubmed-meshheading:12031338-Paclitaxel,
pubmed-meshheading:12031338-Structure-Activity Relationship,
pubmed-meshheading:12031338-Taxoids,
pubmed-meshheading:12031338-Tumor Cells, Cultured
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pubmed:year |
2002
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pubmed:articleTitle |
Synthesis and cytotoxicity of 2alpha-amido docetaxel analogues.
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pubmed:affiliation |
Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, 1 Xian Nong Tan Street, Beijing 100050, PR China. wfang@imm.ac.cn
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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