An inhibitor of the human UDP-GlcNAc 4-epimerase identified from a uridine-based library: a strategy to inhibit O-linked glycosylation.
about
Genome-scale reconstruction of the metabolic network in Staphylococcus aureus N315: an initial draft to the two-dimensional annotation.Structural basis for the acyl chain selectivity and mechanism of UDP-N-acetylglucosamine acyltransferaseDrug targeting Mycobacterium tuberculosis cell wall synthesis: development of a microtiter plate-based screen for UDP-galactopyranose mutase and identification of an inhibitor from a uridine-based library.O-glycan inhibitors generate aryl-glycans, induce apoptosis and lead to growth inhibition in colorectal cancer cell lines.Reconstruction of metabolic pathways for the cattle genome.Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics.Parallel solution-phase synthesis of an adenosine antibiotic analog library.The endoplasmic reticulum-resident chaperone heat shock protein 47 protects the Golgi apparatus from the effects of O-glycosylation inhibition.Synthesis of novel peptidyl adenosine antibiotic analogs.Parallel solution-phase synthesis and general biological activity of a uridine antibiotic analog librarySynthesis and general biological activity of a small adenosine-5'-(carboxamide and sulfanilamide) library.Hydroxybenzaldoximes Are D-GAP-Competitive Inhibitors of E. coli 1-Deoxy-D-Xylulose-5-Phosphate SynthaseGlycan antagonists and inhibitors: a fount for drug discovery.Management of the human mucosal defensive barrier: evidence for glycan legislation.Biosynthetic Machinery Involved in Aberrant Glycosylation: Promising Targets for Developing of Drugs Against CancerDrug-Mediated Regulation of Glycosaminoglycan Biosynthesis.Synthesis and properties of RNAs that contain a PNA-RNA dimer.Towards a better understanding of the substrate specificity of the UDP-N-acetylglucosamine C4 epimerase WbpP.Uracil-directed ligand tethering: an efficient strategy for uracil DNA glycosylase (UNG) inhibitor developmentNine enzymes are required for assembly of the pacidamycin group of peptidyl nucleoside antibioticsMicrowave-assisted synthesis of dinucleoside analogues containing a thiazolidin-4-one linkage via one-pot tandem Staudinger/aza-Wittig/cyclization.Design, Modeling and Synthesis of 1,2,3-Triazole-Linked Nucleoside-Amino Acid Conjugates as Potential Antibacterial Agents.
P2860
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P2860
An inhibitor of the human UDP-GlcNAc 4-epimerase identified from a uridine-based library: a strategy to inhibit O-linked glycosylation.
description
2002 nî lūn-bûn
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2002年の論文
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2002年学术文章
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name
An inhibitor of the human UDP- ...... nhibit O-linked glycosylation.
@en
An inhibitor of the human UDP- ...... nhibit O-linked glycosylation.
@nl
type
label
An inhibitor of the human UDP- ...... nhibit O-linked glycosylation.
@en
An inhibitor of the human UDP- ...... nhibit O-linked glycosylation.
@nl
prefLabel
An inhibitor of the human UDP- ...... nhibit O-linked glycosylation.
@en
An inhibitor of the human UDP- ...... nhibit O-linked glycosylation.
@nl
P1476
An inhibitor of the human UDP- ...... nhibit O-linked glycosylation.
@en
P2093
Carolyn R Bertozzi
Katharine A Winans
P304
P356
10.1016/S1074-5521(02)00093-5
P577
2002-01-01T00:00:00Z