Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
19
|
pubmed:dateCreated |
1976-1-23
|
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.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0006-2960
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
23
|
pubmed:volume |
14
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
4251-4
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:1237309-Acetophenones,
pubmed-meshheading:1237309-Animals,
pubmed-meshheading:1237309-Azides,
pubmed-meshheading:1237309-Binding Sites,
pubmed-meshheading:1237309-Drug Stability,
pubmed-meshheading:1237309-Glyceraldehyde-3-Phosphate Dehydrogenases,
pubmed-meshheading:1237309-Muscles,
pubmed-meshheading:1237309-Photolysis,
pubmed-meshheading:1237309-Protein Binding,
pubmed-meshheading:1237309-Rabbits,
pubmed-meshheading:1237309-Radiation Effects,
pubmed-meshheading:1237309-Ultraviolet Rays
|
pubmed:year |
1975
|
pubmed:articleTitle |
P-Azidophenacyl bromide, a versatile photolabile bifunctional reagent. Reaction with glyceraldehyde-3-phosphate dehydrogenase.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
|