Effect of substitution pattern on 1H, 13C NMR chemical shifts and 1JCH coupling constants in heparin derivatives
- 20 October 2000
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 329 (1) , 239-247
- https://doi.org/10.1016/s0008-6215(00)00144-0
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- 1H and 13C NMR spectral assignments of the major sequences of twelve systematically modified heparin derivativesPublished by Elsevier ,2003
- Carbon-13 and proton magnetic resonance spectra of D-glucose-13CPublished by Elsevier ,2001
- Chemical modifications of heparin that diminish its anticoagulant but preserve its heparanase-inhibitory, angiostatic, anti-tumor and anti-metastatic propertiesGlycobiology, 1996
- Differential effects of the anti-inflammatory compounds heparin, mannose-6-phosphate, and castanospermine on degradation of the vascular basement membrane by leukocytes, endothelial cells, and plateletsJournal of Leukocyte Biology, 1995
- Heparin-like compounds prepared by chemical modification of capsular polysaccharide from E. coli K5Carbohydrate Research, 1994
- More to “heparin” than anticoagulationThrombosis Research, 1994
- Calcium-Dependent Heparin-Like Ligands For L-Selectin in Nonlymphoid Endothelial CellsScience, 1993
- Sulfation of some chemically-modified heparins. Formation of a 3-sulfate analog of heparinCarbohydrate Research, 1991
- “Supersulfated” heparin fragments, a new type of low-molecular weight heparinBiochemical Pharmacology, 1987
- Configurational and conformational influences on the carbon-13 chemical shifts of some carbohydratesCanadian Journal of Chemistry, 1970