Source:http://linkedlifedata.com/resource/pubmed/id/14499570
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
19
|
pubmed:dateCreated |
2003-9-22
|
pubmed:abstractText |
The fluorescence-labelled disaccharides Glcalpha(1-->3)GlcalphaOR and Glcalpha(1-->3)ManalphaOR, both substrates for the glycoprotein-processing enzyme glucosidase II, were synthesised via the use of a n-pentenyl-derived linker at the anomeric position. This allowed incorporation of a pyrenebutyric acid label, via a sequence of oxidative hydroboration, mesylation, azide displacement, reduction with concomitant global deprotection, and peptide coupling. Selective activation of a fully armed thioglycoside in the presence of n-pentenyl glycosides was readily achieved by the use of methyl triflate as promoter.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0008-6215
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
10
|
pubmed:volume |
338
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1937-49
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:14499570-Animals,
pubmed-meshheading:14499570-Carbohydrate Sequence,
pubmed-meshheading:14499570-Chromatography, High Pressure Liquid,
pubmed-meshheading:14499570-Disaccharides,
pubmed-meshheading:14499570-Fluorescence,
pubmed-meshheading:14499570-Liver,
pubmed-meshheading:14499570-Molecular Sequence Data,
pubmed-meshheading:14499570-Molecular Structure,
pubmed-meshheading:14499570-Rats,
pubmed-meshheading:14499570-alpha-Glucosidases
|
pubmed:year |
2003
|
pubmed:articleTitle |
Synthesis of fluorescence-labelled disaccharide substrates of glucosidase II.
|
pubmed:affiliation |
Dyson Perrins Laboratory, Oxford University, South Parks Road, Oxford OX1 3QY, UK.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|