Source:http://linkedlifedata.com/resource/pubmed/id/17630909
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2007-7-16
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pubmed:abstractText |
We synthesized a series of structurally related water-soluble alkyl phenols - sodium 4-hydroxyphenyl propyl sulfonates and thiosulfonates with different number of tert-butyl groups at the ortho-position. In experimental systems of transient metal-induced ethyl oleate and low-density lipoprotein oxidation the antioxidant activity of the compounds increased when the tert-butyl group number at the ortho-position increased and when the sulfonate group was replaced with thiosulfonate. Compounds containing thiosulfonate group in para-propyl substituent also more effectively inhibited reactive oxygen metabolites generated in xanthine-xanthine oxidase system and during morpholinosydnonimine decomposition compared to sulfonate-containing analogs. Phenols with one tert-butyl group at the ortho-position have been shown to exhibit the highest antiinflammatory activity in the model of carrageenan-induced rat paw inflammation, as well as with regard to the expression of the glutathione S-transferase P1-1 gene in HepG2 human hepatoma cell line. Thus, it can be reasonably speculated that the antiinflammatory activity of sulfur-containing phenolic antioxidants in vivo is mediated by their effect on redox-sensitive transcription factors.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Inflammatory Agents...,
http://linkedlifedata.com/resource/pubmed/chemical/Antioxidants,
http://linkedlifedata.com/resource/pubmed/chemical/GSTP1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione S-Transferase pi,
http://linkedlifedata.com/resource/pubmed/chemical/Phenols,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfur Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Water
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0006-2979
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
72
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
644-51
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pubmed:meshHeading |
pubmed-meshheading:17630909-Anti-Inflammatory Agents, Non-Steroidal,
pubmed-meshheading:17630909-Antioxidants,
pubmed-meshheading:17630909-Cell Line,
pubmed-meshheading:17630909-Gene Expression,
pubmed-meshheading:17630909-Glutathione S-Transferase pi,
pubmed-meshheading:17630909-Humans,
pubmed-meshheading:17630909-Inhibitory Concentration 50,
pubmed-meshheading:17630909-Phenols,
pubmed-meshheading:17630909-Solubility,
pubmed-meshheading:17630909-Sulfur Compounds,
pubmed-meshheading:17630909-Water
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pubmed:year |
2007
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pubmed:articleTitle |
Antioxidant and antiinflammatory activity of new water-soluble sulfur-containing phenolic compounds.
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pubmed:affiliation |
Scientific Center of Clinical and Experimental Medicine, Siberian Branch of the Russian Academy of Medical Sciences, Novosibirsk 630117, Russia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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