Muñoz‐García et al., 2012 - Google Patents
Effect of the Substituents of the Neighboring Ring in the Conformational Equilibrium of Iduronate in Heparin‐like TrisaccharidesMuñoz‐García et al., 2012
View PDF- Document ID
- 14925675373367774692
- Author
- Muñoz‐García J
- López‐Prados J
- Angulo J
- Díaz‐Contreras I
- Reichardt N
- de Paz J
- Martín‐Lomas M
- Nieto P
- Publication year
- Publication venue
- Chemistry–A European Journal
External Links
Snippet
Based on the structure of the regular heparin, we have prepared a smart library of heparin‐ like trisaccharides by incorporating some sulfate groups in the sequence α‐d‐GlcNS‐(1‐4)‐ α‐l‐Ido2S‐(1‐4)‐α‐d‐GlcN. According to the 3D structure of heparin, which features one …
- 150000004043 trisaccharides 0 title abstract description 9
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/006—Heteroglycans, i.e. polysaccharides having more than one sugar residue in the main chain in either alternating or less regular sequence; Gellans; Succinoglycans; Arabinogalactans; Tragacanth or gum tragacanth or traganth from Astragalus; Gum Karaya from Sterculia urens; Gum Ghatti from Anogeissus latifolia; Derivatives thereof
- C08B37/0063—Glycosaminoglycans or mucopolysaccharides, e.g. keratan sulfate; Derivatives thereof, e.g. fucoidan
- C08B37/0075—Heparin; Heparan sulfate; Derivatives thereof, e.g. heparosan; Purification or extraction methods thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/006—Heteroglycans, i.e. polysaccharides having more than one sugar residue in the main chain in either alternating or less regular sequence; Gellans; Succinoglycans; Arabinogalactans; Tragacanth or gum tragacanth or traganth from Astragalus; Gum Karaya from Sterculia urens; Gum Ghatti from Anogeissus latifolia; Derivatives thereof
- C08B37/0063—Glycosaminoglycans or mucopolysaccharides, e.g. keratan sulfate; Derivatives thereof, e.g. fucoidan
- C08B37/0069—Chondroitin-4-sulfate, i.e. chondroitin sulfate A; Dermatan sulfate, i.e. chondroitin sulfate B or beta-heparin; Chondroitin-6-sulfate, i.e. chondroitin sulfate C; Derivatives thereof
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Muñoz‐García et al. | Effect of the Substituents of the Neighboring Ring in the Conformational Equilibrium of Iduronate in Heparin‐like Trisaccharides | |
| Perez et al. | Glycosaminoglycans: what remains to be deciphered? | |
| de Paz et al. | The activation of fibroblast growth factors by heparin: Synthesis, structure, and biological activity of heparin‐like oligosaccharides | |
| Holmbeck et al. | The solution conformation of hyaluronan: a combined NMR and molecular dynamics study | |
| US7728589B2 (en) | Method for sequence determination using NMR | |
| Guerrini et al. | Low molecular weight heparins: structural differentiation by bidimensional nuclear magnetic resonance spectroscopy | |
| Tiruchinapally et al. | Divergent heparin oligosaccharide synthesis with preinstalled sulfate esters | |
| Sattelle et al. | A 3D-structural model of unsulfated chondroitin from high-field NMR: 4-sulfation has little effect on backbone conformation | |
| Yates et al. | Effect of substitution pattern on 1H, 13C NMR chemical shifts and 1JCH coupling constants in heparin derivatives | |
| Guerrini et al. | Antithrombin-binding oligosaccharides: structural diversities in a unique function? | |
| Guerrini et al. | Conformational transitions induced in heparin octasaccharides by binding with antithrombin III | |
| Grachev et al. | NMR and conformational studies of linear and cyclic oligo-(1→ 6)-β-D-glucosamines | |
| Guerrini et al. | Low-molecular-weight heparins: differential characterization/physical characterization | |
| Jin et al. | Residual dipolar coupling investigation of a heparin tetrasaccharide confirms the limited effect of flexibility of the iduronic acid on the molecular shape of heparin | |
| Mobli et al. | The structural plasticity of heparan sulfate NA-domains and hence their role in mediating multivalent interactions is confirmed by high-accuracy 15N-NMR relaxation studies | |
| Han et al. | Monosaccharide compositions of sulfated chitosans obtained by analysis of nitrous acid degraded and pyrazolone-labeled products | |
| Iacomini et al. | “Linkage region” sequences of heparins and heparan sulfates: detection and quantification by nuclear magnetic resonance spectroscopy | |
| Malavaki et al. | Heparan sulfate: biological significance, tools for biochemical analysis and structural characterization | |
| Gabrielli et al. | Molecular recognition of natural and non‐natural substrates by cellodextrin phosphorylase from Ruminiclostridium thermocellum investigated by NMR spectroscopy | |
| de Paz et al. | Synthesis and biological evaluation of a heparin‐like hexasaccharide with the structural motifs for binding to FGF and FGFR | |
| Balogh et al. | Conformational analysis of heparin-analogue pentasaccharides by nuclear magnetic resonance spectroscopy and molecular dynamics simulations | |
| Limtiaco et al. | NMR methods to monitor the enzymatic depolymerization of heparin | |
| Guo et al. | Advancing MS n spatial resolution and documentation for glycosaminoglycans by sulfate-isotope exchange | |
| Chevalier et al. | The Heparin− Ca2+ interaction: structure of the Ca2+ binding site | |
| Silipo et al. | Conformational analysis of a dermatan sulfate‐derived tetrasaccharide by NMR, molecular modeling, and residual dipolar couplings |