C-Fucopeptides as selectin antagonists: Attachment of lipid moieties enhances the activity
- 9 December 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (50) , 9033-9036
- https://doi.org/10.1016/s0040-4039(96)02121-1
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- An efficient chemo-enzymatic synthesis of α-amino-β-hydroxy-γ-butyrolactonePublished by Elsevier ,2000
- Studies on Selectin Blocker. 1. Structure−Activity Relationships of Sialyl Lewis X AnalogsJournal of Medicinal Chemistry, 1996
- Synthesis and biological activity of conformationally constrained sialyl Lewis X analogues with reduced carbohydrate characterBioorganic & Medicinal Chemistry Letters, 1996
- Sialyl Lewis x Liposomes as a Multivalent Ligand and Inhibitor of E-Selectin Mediated Cellular AdhesionJournal of the American Chemical Society, 1996
- Spiroketal glycomimetics: the synthesis of a conformationally restrained Sialyl Lewis X mimicBioorganic & Medicinal Chemistry Letters, 1995
- Design and Synthesis of Sialyl Lewis X MimeticsJournal of the American Chemical Society, 1995
- Catalytic Asymmetric DihydroxylationChemical Reviews, 1994
- Traffic signals for lymphocyte recirculation and leukocyte emigration: The multistep paradigmCell, 1994
- Structure--function studies on selectin carbohydrate ligands. Modifications to fucose, sialic acid and sulphate as a sialic acid replacementGlycobiology, 1993
- New ligands double the scope of the catalytic asymmetric dihydroxylation of olefinsThe Journal of Organic Chemistry, 1991