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O-glycosylation (NeuAcα2-6GalNAc) at Thr131 and Thr144
CMP-Sialic acid is utilized to study and manipulate glycosylation patterns of proteins and lipids
C15H27N3O11 / 425
/ Fmoc-Thr(Neu5Acα(2-6)GalNAc)-OH (Peracetate
Gal-Ser deprotected(Free NH
GA521005: Fmoc-Ser(Glc(Ac)4-α-D)-OH Pack Size:100 mg O-glycosylation (NeuAcα2-6GalNAc) at Thr131 andC32H35NO14 657. 62 An Fmoc protected L serine building block carrying an D glucose residue, designed for solid phase peptide synthesis (SPPS) of glycopeptides. The N Fmoc group is removed under standard base conditions (piperidine) during chain elongation, while the free carboxylic acid is available for coupling to the growing resin bound peptide. The sugar hydroxyl groups are protected as four acetate esters (Ac4), which keep the glycan inert during
