Source:http://linkedlifedata.com/resource/pubmed/id/18680358
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
16
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pubmed:dateCreated |
2008-8-25
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pubmed:abstractText |
On the basis of the structure of somatostatin analogue TT-232 (1), which exhibited a highly potent antitumor activity, we synthesized small linear peptide derivatives and evaluated their antitumor and apoptotic activity. Of them, Boc-Tyr-D-Trp-1-adamantylamide (5) had the most potent cell antiproliferative activity in SW480 and A431 cell lines, which was supported in A431 cell lines by FACS analysis that demonstrated a major increase in DNA fragmentation in the subG1 fraction.
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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 |
Aug
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pubmed:issn |
1520-4804
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
28
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5121-4
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pubmed:meshHeading |
pubmed-meshheading:18680358-Adamantane,
pubmed-meshheading:18680358-Antineoplastic Agents,
pubmed-meshheading:18680358-Apoptosis,
pubmed-meshheading:18680358-Cell Proliferation,
pubmed-meshheading:18680358-Humans,
pubmed-meshheading:18680358-Somatostatin,
pubmed-meshheading:18680358-Tumor Cells, Cultured
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pubmed:year |
2008
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pubmed:articleTitle |
Synthesis of somatostatin analogues containing C-terminal adamantane and their antiproliferative properties.
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pubmed:affiliation |
Faculty of Pharmaceutical Sciences, Department of Medicinal Chemistry, Kobe Gakuin University, Nishi-ku, Kobe, 651-2180, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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