Search Results - "Ramphal, John"
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Total synthesis of trifluorobutyryl-modified, protected sialyl Lewis X by a convergent [2+2] approach
Published in Tetrahedron letters (01-01-2015)“…[Display omitted] Structural and quantitative changes in the expression of sialic acid residues on the surface of eukaryotic cells profoundly influence a broad…”
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Total synthesis of trifluorobutyryl-modified, globally protected sialyl Lewis x by a convergent [2+2] approach
Published in Tetrahedron letters (01-01-2015)“…Structural and quantitative changes in the expression of sialic acid residues on the surface of eukaryotic cells profoundly influence a broad range of…”
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Galactokinase 1 is the source of elevated galactose‐1‐phosphate and cerebrosides are modestly reduced in a mouse model of classic galactosemia
Published in JIMD reports (01-07-2024)“…Classic galactosemia (CG) arises from loss‐of‐function mutations in the Galt gene, which codes for the enzyme galactose‐1‐phosphate uridylyltransferase (GALT),…”
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Structure-Based design and discovery of novel inhibitors of protein tyrosine phosphatases
Published in Bioorganic & medicinal chemistry (17-04-2003)“…Protein tyrosine phosphatases (PTPs) are important in the regulation of signal transduction processes. Certain enzymes of this class are considered as…”
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Structure-Activity Relationships of Sialyl Lewis x-Containing Oligosaccharides. 1. Effect of Modifications of the Fucose Moiety
Published in Journal of medicinal chemistry (01-10-1994)“…Leukocyte adhesion to the vasculature is mediated by E-, P-, and L-selectins. The natural ligands for E- and P-selectins have not been fully characterized but…”
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Ligand Interactions with E-Selectin. Identification of a New Binding Site for Recognition of N-Acyl Aromatic Glucosamine Substituents of Sialyl Lewis X
Published in Journal of medicinal chemistry (29-03-1996)“…Several N-acylglucosamine derivatives of sialyl Lewis X (1−3) were prepared using a combined chemical enzymatic approach and evaluated as an inhibitor of…”
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A selective small molecule inhibitor of c-Met kinase inhibits c-met-dependent phenotypes in vitro and exhibits cytoreductive antitumor activity in vivo
Published in Cancer research (Chicago, Ill.) (01-11-2003)“…The c-Met receptor tyrosine kinase and its ligand, hepatocyte growth factor (HGF), have been implicated in the development and progression of several human…”
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Design, synthesis, and SAR of 2-dialkylamino-4-arylpyrimidines as potent and selective corticotropin-releasing factor(1) (CRF(1)) receptor antagonists
Published in Bioorganic & medicinal chemistry letters (03-05-2004)“…A series of 2-dialkylamino-4-phenylpyrimidines (7) was designed and synthesized as CRF(1) antagonists. SAR studies of this series resulted in the discovery of…”
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The Reactions of o-Quinone Monoimides with Some Thiophenes and Furans
Published in Heterocycles (01-05-1993)Get full text
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