| pubmed-article:9824283 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9824283 | lifeskim:mentions | umls-concept:C0007413 | lld:lifeskim |
| pubmed-article:9824283 | lifeskim:mentions | umls-concept:C0136157 | lld:lifeskim |
| pubmed-article:9824283 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:9824283 | pubmed:dateCreated | 1998-12-10 | lld:pubmed |
| pubmed-article:9824283 | pubmed:abstractText | Nitration of phenolic compounds is a well-established mechanism on interaction with peroxynitrite. However, while nitration is the predominant reaction for monophenolic hydroxycinnamates, this does not take place with the catechol-containing hydroxycinnamate, caffeic acid. The aim of the present study was to investigate the mechanism of the chemical interaction of caffeic acid with peroxynitrite and to characterise the products formed. A novel compound was detected and characterised as the o-quinone of caffeic acid based on its reaction with nucleophilic thiol compounds, glutathione and L-cysteine. The same novel product was identified following the oxidation of caffeic acid in alkaline solutions confirming the identity of this species as a caffeic acid oxidation product. | lld:pubmed |
| pubmed-article:9824283 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9824283 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9824283 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9824283 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9824283 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:9824283 | pubmed:issn | 0014-5793 | lld:pubmed |
| pubmed-article:9824283 | pubmed:author | pubmed-author:Rice-EvansCC | lld:pubmed |
| pubmed-article:9824283 | pubmed:author | pubmed-author:KerryNN | lld:pubmed |
| pubmed-article:9824283 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9824283 | pubmed:day | 23 | lld:pubmed |
| pubmed-article:9824283 | pubmed:volume | 437 | lld:pubmed |
| pubmed-article:9824283 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9824283 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9824283 | pubmed:pagination | 167-71 | lld:pubmed |
| pubmed-article:9824283 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:meshHeading | pubmed-meshheading:9824283-... | lld:pubmed |
| pubmed-article:9824283 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9824283 | pubmed:articleTitle | Peroxynitrite oxidises catechols to o-quinones. | lld:pubmed |
| pubmed-article:9824283 | pubmed:affiliation | Antioxidant Research Centre, Guy's, King's College and St. Thomas's School of Biomedical Sciences, London, UK. | lld:pubmed |
| pubmed-article:9824283 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9824283 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9824283 | lld:pubmed |
