pubmed-article:11249126 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11249126 | lifeskim:mentions | umls-concept:C0441655 | lld:lifeskim |
pubmed-article:11249126 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
pubmed-article:11249126 | lifeskim:mentions | umls-concept:C0015196 | lld:lifeskim |
pubmed-article:11249126 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
pubmed-article:11249126 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
pubmed-article:11249126 | lifeskim:mentions | umls-concept:C0205460 | lld:lifeskim |
pubmed-article:11249126 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:11249126 | pubmed:dateCreated | 2001-3-15 | lld:pubmed |
pubmed-article:11249126 | pubmed:abstractText | Fourteen novel C-prenylated and O-allylated 1,3-diarylpropenones (chalcones) were synthesized by Claisen-Schmidt condensation reaction of C-prenylated/O-allylated acetophenones with appropriate aldehydes; twelve of these model chalcones were screened in an assay based on the confrontation of invasive human MCF-7/6 mammary carcinoma cells with fragments of normal embryonic chick heart in vitro. Out of the twelve chalcones tested, three were found to exhibit potent anti-invasive activity. Some of these chalcones and their precursor acetophenones were also tested for inhibition of initiation of lipid peroxidation in rat liver microsomes; a prenylated acetophenone carrying two methoxy groups and two free phenolic hydroxy functions was found to be a potential antioxidant. | lld:pubmed |
pubmed-article:11249126 | pubmed:language | eng | lld:pubmed |
pubmed-article:11249126 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11249126 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11249126 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11249126 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11249126 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11249126 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11249126 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11249126 | pubmed:month | Feb | lld:pubmed |
pubmed-article:11249126 | pubmed:issn | 0968-0896 | lld:pubmed |
pubmed-article:11249126 | pubmed:author | pubmed-author:JainS CSC | lld:pubmed |
pubmed-article:11249126 | pubmed:author | pubmed-author:MukherjeeSS | lld:pubmed |
pubmed-article:11249126 | pubmed:author | pubmed-author:KumarVV | lld:pubmed |
pubmed-article:11249126 | pubmed:author | pubmed-author:OlsenC ECE | lld:pubmed |
pubmed-article:11249126 | pubmed:author | pubmed-author:ICER MRM | lld:pubmed |
pubmed-article:11249126 | pubmed:author | pubmed-author:PrasadA KAK | lld:pubmed |
pubmed-article:11249126 | pubmed:author | pubmed-author:ParmarV SVS | lld:pubmed |
pubmed-article:11249126 | pubmed:author | pubmed-author:BrackeM EME | lld:pubmed |
pubmed-article:11249126 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11249126 | pubmed:volume | 9 | lld:pubmed |
pubmed-article:11249126 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11249126 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11249126 | pubmed:pagination | 337-45 | lld:pubmed |
pubmed-article:11249126 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:11249126 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11249126 | pubmed:articleTitle | Synthetic and biological activity evaluation studies on novel 1,3-diarylpropenones. | lld:pubmed |
pubmed-article:11249126 | pubmed:affiliation | Department of Chemistry, University of Delhi, India. | lld:pubmed |
pubmed-article:11249126 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11249126 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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