rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
9
|
pubmed:dateCreated |
2008-5-5
|
pubmed:abstractText |
Compounds 2a- h and 6 displayed significant GI 50 values of 10(-7)-10(-6) M against various cancer cell lines. Of these compounds, 2-(6-(2-trifluoromethylphenyl))-3(Z)-hexen-1,5-diynyl)aniline (2c) showed the most potent growth inhibition activity. Compound 2c also arrested cancer cells in the G2/M phase and in low concentration reduced a significant percentage of MDA-MB-231/ATCC breast cancer tetraploid cells. In addition to the G2/M block, compound 2c caused microtubule depolymerization and induced apoptosis via activation of the caspase family.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0022-2623
|
pubmed:author |
pubmed-author:ChangLong-SenLS,
pubmed-author:DuhTsai-HuiTH,
pubmed-author:HongYi-RenYR,
pubmed-author:LinChi-FongCF,
pubmed-author:LinChing-ChihCC,
pubmed-author:LinShinne-RenSR,
pubmed-author:LinYing-TingYT,
pubmed-author:LoYu-HsiangYH,
pubmed-author:WuMing-JungMJ,
pubmed-author:YangSheng-HueiSH,
pubmed-author:YangShyh-ChyunSC
|
pubmed:issnType |
Print
|
pubmed:day |
8
|
pubmed:volume |
51
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2682-8
|
pubmed:meshHeading |
pubmed-meshheading:18386884-Aniline Compounds,
pubmed-meshheading:18386884-Biopolymers,
pubmed-meshheading:18386884-Cell Cycle,
pubmed-meshheading:18386884-Cell Line, Tumor,
pubmed-meshheading:18386884-Cell Proliferation,
pubmed-meshheading:18386884-Drug Screening Assays, Antitumor,
pubmed-meshheading:18386884-Humans,
pubmed-meshheading:18386884-Microtubules,
pubmed-meshheading:18386884-Stereoisomerism,
pubmed-meshheading:18386884-Structure-Activity Relationship,
pubmed-meshheading:18386884-Tubulin,
pubmed-meshheading:18386884-Tubulin Modulators
|
pubmed:year |
2008
|
pubmed:articleTitle |
2-(6-aryl-3(Z)-hexen-1,5-diynyl)anilines as a new class of potent antitubulin agents.
|
pubmed:affiliation |
Graduate Institute of Pharmaceutical Sciences, Graduate Institute of Biochemistry, Kaohsiung Medical University, Kaohsiung, Taiwan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|