| pubmed-article:10328301 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C0684339 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C0330302 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C0007009 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C0024485 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C0054858 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C1708632 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C0243071 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C0449445 | lld:lifeskim |
| pubmed-article:10328301 | lifeskim:mentions | umls-concept:C1522485 | lld:lifeskim |
| pubmed-article:10328301 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:10328301 | pubmed:dateCreated | 1999-8-3 | lld:pubmed |
| pubmed-article:10328301 | pubmed:abstractText | A 13-C labeled water soluble derivative of alkylcatechol was synthesized and reacted with human serum albumin in phosphate buffer at pH 7.4 in air to allow a slow oxidation of the catechol into orthoquinone. The formation of several adducts was evidenced by a combination of 13C and 1H-13C correlation NMR. Although some adducts could result from a classical o-quinone formation - Michael type addition, our results suggest that a second pathway, involving a direct reaction of a carbon centered radical with proteins could be an important mechanism in the formation of modified proteins. | lld:pubmed |
| pubmed-article:10328301 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10328301 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10328301 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:10328301 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10328301 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10328301 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10328301 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10328301 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10328301 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10328301 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:10328301 | pubmed:issn | 0960-894X | lld:pubmed |
| pubmed-article:10328301 | pubmed:author | pubmed-author:GoetzGG | lld:pubmed |
| pubmed-article:10328301 | pubmed:author | pubmed-author:LepoittevinJ... | lld:pubmed |
| pubmed-article:10328301 | pubmed:author | pubmed-author:MeschkatEE | lld:pubmed |
| pubmed-article:10328301 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10328301 | pubmed:day | 19 | lld:pubmed |
| pubmed-article:10328301 | pubmed:volume | 9 | lld:pubmed |
| pubmed-article:10328301 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10328301 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10328301 | pubmed:pagination | 1141-6 | lld:pubmed |
| pubmed-article:10328301 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:10328301 | pubmed:meshHeading | pubmed-meshheading:10328301... | lld:pubmed |
| pubmed-article:10328301 | pubmed:meshHeading | pubmed-meshheading:10328301... | lld:pubmed |
| pubmed-article:10328301 | pubmed:meshHeading | pubmed-meshheading:10328301... | lld:pubmed |
| pubmed-article:10328301 | pubmed:meshHeading | pubmed-meshheading:10328301... | lld:pubmed |
| pubmed-article:10328301 | pubmed:meshHeading | pubmed-meshheading:10328301... | lld:pubmed |
| pubmed-article:10328301 | pubmed:meshHeading | pubmed-meshheading:10328301... | lld:pubmed |
| pubmed-article:10328301 | pubmed:meshHeading | pubmed-meshheading:10328301... | lld:pubmed |
| pubmed-article:10328301 | pubmed:meshHeading | pubmed-meshheading:10328301... | lld:pubmed |
| pubmed-article:10328301 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10328301 | pubmed:articleTitle | Synthesis of a water-soluble analog of 6-methyl-3-N-alkyl catechol labeled with carbon 13: NMR approach to the reactivity of poison ivy/oak sensitizers toward proteins. | lld:pubmed |
| pubmed-article:10328301 | pubmed:affiliation | Laboratoire de Dermatochimie associé au CNRS, Université Louis Pasteur, Clinique Dermatologique, CHU, Strasbourg, France. | lld:pubmed |
| pubmed-article:10328301 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10328301 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
