0000000000597876

AUTHOR

Markus Rösch

showing 3 related works from this author

Synthetic Inhibitors of Cell Adhesion: A Glycopeptide from E-Selectin Ligand 1 (ESL-1) with the Arabino Sialyl Lewisx Structure

2001

Particularly selective methods are required for the synthesis of arabino sialyl Lewisx glycopeptides owing to the acid-labile β-arabinopyranoside bond. It is important for the inhibition of cell adhesion that the arabino sialyl Lewisx glycopeptide 1, which contains the Gly 672 -Asp 681 sequence of the E-selectin Ligand 1 (ESL-1), binds ten times more strongly than sialyl Lewisx to E-selectin, although it is monovalent and does not contain L-fucose, which is considered essential.

carbohydrates (lipids)Solid-phase synthesisBiochemistryChemistryembryonic structuresGeneral ChemistryE-selectin ligand-1Cell adhesionLigand (biochemistry)CatalysisGlycopeptideAngewandte Chemie International Edition
researchProduct

Synthetische Inhibitoren der Zelladhäsion: ein Glycopeptid aus dem E-Selektin-Liganden 1 (ESL-1) mit Arabino-Sialyl-Lewisx-Struktur

2001

ChemistryStereochemistryGeneral MedicineGlycopeptideAngewandte Chemie
researchProduct

ChemInform Abstract: Glycoconjugates as Tumor-Associated Antigens and Ligands in Regulatory Processes

2010

chemistry.chemical_classificationchemistryBiochemistryGlycoconjugateStereochemistryGeneral MedicineTumor associated antigenChemInform
researchProduct