Lysine-based Cluster Mannosides That Inhibit Ligand Binding to the Human Mannose Receptor at Nanomolar Concentration
Open Access
- 1 November 1996
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 271 (45) , 28024-28030
- https://doi.org/10.1074/jbc.271.45.28024
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Synthesis of Cluster Galactosides with High Affinity for the Hepatic Asialoglycoprotein ReceptorJournal of Medicinal Chemistry, 1995
- Mechanisms of Tissue‐type Plasminogn Activator (tPA) Clearance by the LiveraAnnals of the New York Academy of Sciences, 1992
- Isolation and Characterization of the Mannose Receptor From Human Liver Potentially Involved in the Plasma Clearance of Tissue–Type Plasminogen ActivatorHepatology, 1992
- Uptake of Pneumocystis carinii mediated by the macrophage mannose receptorNature, 1991
- Molecular characterization of the human macrophage mannose receptor: demonstration of multiple carbohydrate recognition-like domains and phagocytosis of yeasts in Cos-1 cells.The Journal of Experimental Medicine, 1990
- Muramyl dipeptide bound to poly-l-lysine substituted with mannose and gluconoyl residues as macrophage activatorsGlycoconjugate Journal, 1989
- Synthetic neoglycoproteins: a class of regents for detection of sugar-recognizing substances.Journal of Histochemistry & Cytochemistry, 1984
- Accumulation of a nondegradable mannose ligand within rabbit alveolar macrophages. Receptor reutilization is independent of ligand degradationBiochemistry, 1984
- Selective inhibition by monosaccharides of tumor cell cytotoxicity mediated by mouse macrophages, macrophage‐like cell lines, and natural killer cellsInternational Journal of Cancer, 1983
- Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a,6a-diphenylglycolurilBiochemical and Biophysical Research Communications, 1978