rdf:type |
|
lifeskim:mentions |
umls-concept:C0003693,
umls-concept:C0023823,
umls-concept:C0056244,
umls-concept:C0127400,
umls-concept:C0243072,
umls-concept:C0243077,
umls-concept:C0332120,
umls-concept:C0441712,
umls-concept:C1158919,
umls-concept:C1554184,
umls-concept:C1704419
|
pubmed:issue |
8
|
pubmed:dateCreated |
1994-11-17
|
pubmed:abstractText |
1'-Hydroxyeugenol- and epoxy-Z-coniferyl alcohol esters from Coreopsis species as well as synthetic derivatives of these natural compounds were examined as lipoxygenase inhibitors and as LDL (low density lipoprotein)-stabilizing agents. Most of the compounds displayed inhibitory activity on the formation of leukotrienes (LTB4 and LTC4) in a cellular (RBL-1 cells) assay as well as in a cell-free 5-lipoxygenase assay at concentrations of 4-24 mumol/l. No effect of selected compounds was observed on mammalian lipoxygenases with other specificity (12- and 15-lipoxygenase). The more lipophilic derivatives also effectively reduced Cu(2+)-mediated oxidation of LDL. The findings are discussed on the base of structure-activity relationships.
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pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Arachidonate 12-Lipoxygenase,
http://linkedlifedata.com/resource/pubmed/chemical/Arachidonate 15-Lipoxygenase,
http://linkedlifedata.com/resource/pubmed/chemical/Arachidonate 5-Lipoxygenase,
http://linkedlifedata.com/resource/pubmed/chemical/Copper,
http://linkedlifedata.com/resource/pubmed/chemical/Eugenol,
http://linkedlifedata.com/resource/pubmed/chemical/Leukotriene B4,
http://linkedlifedata.com/resource/pubmed/chemical/Leukotriene C4,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoxygenase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Phenols,
http://linkedlifedata.com/resource/pubmed/chemical/coniferyl alcohol
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
|
pubmed:issn |
0004-4172
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pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
44
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
956-61
|
pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:7945541-Animals,
pubmed-meshheading:7945541-Arachidonate 12-Lipoxygenase,
pubmed-meshheading:7945541-Arachidonate 15-Lipoxygenase,
pubmed-meshheading:7945541-Arachidonate 5-Lipoxygenase,
pubmed-meshheading:7945541-Copper,
pubmed-meshheading:7945541-Eugenol,
pubmed-meshheading:7945541-Humans,
pubmed-meshheading:7945541-Leukemia, Basophilic, Acute,
pubmed-meshheading:7945541-Leukotriene B4,
pubmed-meshheading:7945541-Leukotriene C4,
pubmed-meshheading:7945541-Lipoproteins,
pubmed-meshheading:7945541-Lipoxygenase Inhibitors,
pubmed-meshheading:7945541-Oxidation-Reduction,
pubmed-meshheading:7945541-Phenols,
pubmed-meshheading:7945541-Rats,
pubmed-meshheading:7945541-Structure-Activity Relationship,
pubmed-meshheading:7945541-Tumor Cells, Cultured
|
pubmed:year |
1994
|
pubmed:articleTitle |
1'-Hydroxyeugenol- and coniferyl alcohol derivatives as effective inhibitors of 5-lipoxygenase and Cu(2+)-mediated low density lipoprotein oxidation. Evidence for a dual mechanism.
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pubmed:affiliation |
Pharmazeutisch-Chemisches Institut, Universität Heidelberg, Fed. Rep. of Germany.
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pubmed:publicationType |
Journal Article
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