A UNIQUE AND HIGHLY FACILE METHOD FOR SYNTHESIZING DISULFIDE-LINKED NEOGLYCOCONJUGATES - A NEW APPROACH FOR REMODELING OF PEPTIDES AND PROTEINS

Authors
MACINDOE WM VANOIJEN AH BOONS GJ
Citation
Wm. Macindoe et al., A UNIQUE AND HIGHLY FACILE METHOD FOR SYNTHESIZING DISULFIDE-LINKED NEOGLYCOCONJUGATES - A NEW APPROACH FOR REMODELING OF PEPTIDES AND PROTEINS, Chemical communications, (7), 1998, pp. 847-848
Citations number
20
Categorie Soggetti
Chemistry
Journal title
Chemical communications → ACNP
ISSN journal
13597345
Issue
7
Year of publication
1998
Pages
847 - 848
Database
ISI
SICI code
1359-7345(1998):7<847:AUAHFM>2.0.ZU;2-F
Abstract
An asymmetric disulfide linkage, formed by conjugation of a 5-nitropyr idine-2-sulfenyl activated thioglycoside and a protein or pre-assemble d peptide sequence, represents a good structural mimic of natural aspa ragine glycosylation.