Source:http://linkedlifedata.com/resource/pubmed/id/20846760
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2010-10-11
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pubmed:abstractText |
A series of substituted 2-phenylthiazole-4-carboxamide derivatives were synthesized as potential cytotoxic agents and evaluated against three human cancer cell lines including T47D (Breast cancer), Caco-2 (Colorectal cancer) and HT-29 (Colon cancer). The SAR of the arylacetamido pendent connected to the para-position of 2-phenylthiazole were explored. It was found that substitution at the 4-position by a methoxy group led to improvement of activity against Caco-2 cells while 2-methoxy substituent could maintain the high activity against HT-29 and T47D cell lines. Also, 3-fluoro analog showed good cytotoxic activity profile against all cell lines with IC(50) values less than 10 ?g/mL.
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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 |
Nov
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pubmed:issn |
1768-3254
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Masson SAS. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5384-9
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pubmed:meshHeading |
pubmed-meshheading:20846760-Amides,
pubmed-meshheading:20846760-Antineoplastic Agents,
pubmed-meshheading:20846760-Cell Line, Tumor,
pubmed-meshheading:20846760-Humans,
pubmed-meshheading:20846760-Magnetic Resonance Spectroscopy,
pubmed-meshheading:20846760-Mass Spectrometry,
pubmed-meshheading:20846760-Spectrophotometry, Infrared,
pubmed-meshheading:20846760-Structure-Activity Relationship,
pubmed-meshheading:20846760-Thiazolidines
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pubmed:year |
2010
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pubmed:articleTitle |
Synthesis and biological evaluation of 2-phenylthiazole-4-carboxamide derivatives as anticancer agents.
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pubmed:affiliation |
Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 14174, Iran.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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