Abstract
Our recent studies have revealed the existence of two distinct Gal: 3-O-sulfotransferases capable of acting on the C-3 position of galactose in a Core 2 branched structure, e.g., Galβ1→4GlcNAcβ1→6(Galβ1→3)GalNacα1→OBenzyl as acceptor to give 3-O-sulfoGalβ1→4GlcNAcβ1→3(Galβ1→3)GalNAcα1→OB 20 and Galβ1→4GlcNAcβ1→6(3-O-sulfoGalβ1→3)GalNAcα1→OB 23. We herein report the synthesis of these two compounds and also that of other modified analogs that are highly specific acceptors for the two sulfotransferases. Appropriately protected 1-thio-glycosides 7, 8, and 10 were employed as glycosyl donors for the synthesis of our target compounds.
| Original language | English |
|---|---|
| Pages (from-to) | 951-959 |
| Number of pages | 9 |
| Journal | Glycoconjugate Journal |
| Volume | 15 |
| Issue number | 10 |
| DOIs | |
| State | Published - 1998 |
Keywords
- Acceptors
- Oligosaccharides
- Sulfotransferases
- Synthetic
Fingerprint
Dive into the research topics of 'Synthesis of Gal-β-(1→4)-GlcNAc-β-(1→6)-[Gal-β-(1→3)]-GalNAc-α-OBn oligosaccharides bearing O-methyl or O-sulfo groups at C-3 of the Gal residue: Specific acceptors for Gal: 3-O-sulfotransferases'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver