pubmed-article:1237309 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1237309 | lifeskim:mentions | umls-concept:C0017857 | lld:lifeskim |
pubmed-article:1237309 | lifeskim:mentions | umls-concept:C0443286 | lld:lifeskim |
pubmed-article:1237309 | lifeskim:mentions | umls-concept:C1414968 | lld:lifeskim |
pubmed-article:1237309 | lifeskim:mentions | umls-concept:C0034760 | lld:lifeskim |
pubmed-article:1237309 | lifeskim:mentions | umls-concept:C0048092 | lld:lifeskim |
pubmed-article:1237309 | pubmed:issue | 19 | lld:pubmed |
pubmed-article:1237309 | pubmed:dateCreated | 1976-1-23 | lld:pubmed |
pubmed-article:1237309 | pubmed:abstractText | The synthesis of the photochemically labile bifunctional reagent p-azidophenacyl bromide (1) is described. This compound may be covalently attached to a known site of an enzyme or other macromolecule by nucleophilic displacement at the alpha-bromo ketone moiety. Subsequent irradiation of the bound reagent gives a nitrene which may insert into a second portion of the enzyme forming a cross-link. Regeant 1 proved to be an excellent inhibitor of rabbit muscle glyceraldehyde-3-phosphate dehydrogenase. | lld:pubmed |
pubmed-article:1237309 | pubmed:language | eng | lld:pubmed |
pubmed-article:1237309 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1237309 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:1237309 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1237309 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1237309 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1237309 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1237309 | pubmed:month | Sep | lld:pubmed |
pubmed-article:1237309 | pubmed:issn | 0006-2960 | lld:pubmed |
pubmed-article:1237309 | pubmed:author | pubmed-author:HixsonS SSS | lld:pubmed |
pubmed-article:1237309 | pubmed:author | pubmed-author:HixsonS HSH | lld:pubmed |
pubmed-article:1237309 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1237309 | pubmed:day | 23 | lld:pubmed |
pubmed-article:1237309 | pubmed:volume | 14 | lld:pubmed |
pubmed-article:1237309 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1237309 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1237309 | pubmed:pagination | 4251-4 | lld:pubmed |
pubmed-article:1237309 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:1237309 | pubmed:meshHeading | pubmed-meshheading:1237309-... | lld:pubmed |
pubmed-article:1237309 | pubmed:year | 1975 | lld:pubmed |
pubmed-article:1237309 | pubmed:articleTitle | P-Azidophenacyl bromide, a versatile photolabile bifunctional reagent. Reaction with glyceraldehyde-3-phosphate dehydrogenase. | lld:pubmed |
pubmed-article:1237309 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1237309 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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