rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
8
|
pubmed:dateCreated |
2002-4-4
|
pubmed:abstractText |
Potential E- and P-selectin inhibitors were synthesized to explore a hydrophobic area on the E-selectin surface and the PSGL-1 protein binding site on the P-selectin surface that was recently defined by crystallography. Three series of mannose-based compounds (libraries A, B, and C) were synthesized using solution phase parallel synthesis. Biological evaluation of these compounds was done using two ELISA-based assays and transferred NOE (trNOE) experiments. Some of the compounds showed better activity than sLe(x) in the P-selectin assay.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0022-2623
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
11
|
pubmed:volume |
45
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1563-6
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:11931610-Combinatorial Chemistry Techniques,
pubmed-meshheading:11931610-Crystallography, X-Ray,
pubmed-meshheading:11931610-E-Selectin,
pubmed-meshheading:11931610-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:11931610-Humans,
pubmed-meshheading:11931610-Ligands,
pubmed-meshheading:11931610-Magnetic Resonance Spectroscopy,
pubmed-meshheading:11931610-Mannosides,
pubmed-meshheading:11931610-Membrane Glycoproteins,
pubmed-meshheading:11931610-Models, Molecular,
pubmed-meshheading:11931610-Oligosaccharides,
pubmed-meshheading:11931610-P-Selectin,
pubmed-meshheading:11931610-Protein Binding,
pubmed-meshheading:11931610-Structure-Activity Relationship
|
pubmed:year |
2002
|
pubmed:articleTitle |
Beta-C-mannosides as selectin inhibitors.
|
pubmed:affiliation |
Department of Chemical Sciences, Wyeth Research, 200 Cambridge Park Drive, Cambridge, Massachusetts 02140, USA. nkaila@war.wyeth.com
|
pubmed:publicationType |
Journal Article,
Comparative Study
|