Source:http://linkedlifedata.com/resource/pubmed/id/16236451
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2005-12-19
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pubmed:abstractText |
Curcumin (1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione, 1) is a yellow ingredient isolated from turmeric (curcumin longa). It has been shown to exhibit a variety of biological activities including antioxidative activity. In order to find more active antioxidants with 1 as the lead compound we synthesized curcumin analogues, i.e., 1-(3,4-dihydroxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione (2), 1-(4-hydroxy-3-methoxyphenyl)-7-(4-hydroxyphenyl)-1,6-heptadiene-3,5-dione (3), 1,7-bis-(4-hydroxyphenyl)-1,6-heptadiene-3,5-dione (4), 1-(3,4-dimethoxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione (5), 1,7-bis(3,4-dimethoxyphenyl)-1,6-heptadiene-3,5-dione (6), and 1,7-diphenyl-1,6-heptadiene-3,5-dione (7), and evaluated their antioxidative activity. The in vitro oxidative damage to both lipids and proteins in rat liver mitochondria was used as a model to study the free radical-induced oxidative damage of biological lipids as well as proteins and the protective effects of these curcumin analogues. It was found that these compounds, except 6 and 7, could effectively inhibit the free radical induced lipid peroxidation and protein oxidative damage of rat liver mitochondria by H-atom abstraction from the phenolic groups. Compound 2 which bear ortho-diphenoxyl functionality exhibited remarkably higher antioxidative activity for lipids and proteins than curcumin and other analogues, and the 4-hydroxy-3-methoxyphenyl group also play an important role in the antioxidative activity.
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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 |
Jan
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pubmed:issn |
0006-3002
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
1760
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
70-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16236451-Animals,
pubmed-meshheading:16236451-Antioxidants,
pubmed-meshheading:16236451-Curcumin,
pubmed-meshheading:16236451-Female,
pubmed-meshheading:16236451-Kinetics,
pubmed-meshheading:16236451-Lipid Peroxidation,
pubmed-meshheading:16236451-Mitochondria, Liver,
pubmed-meshheading:16236451-Oxidation-Reduction,
pubmed-meshheading:16236451-Proteins,
pubmed-meshheading:16236451-Rats,
pubmed-meshheading:16236451-Rats, Wistar,
pubmed-meshheading:16236451-Structure-Activity Relationship,
pubmed-meshheading:16236451-Thiobarbituric Acid Reactive Substances
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pubmed:year |
2006
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pubmed:articleTitle |
Inhibition of lipid peroxidation and protein oxidation in rat liver mitochondria by curcumin and its analogues.
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pubmed:affiliation |
National Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou, Gansu 730,000, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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