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Fmoc-Ser(β-D-GlcNAc(Ac)3-(1-3)-α-D-GalNAc(Ac)2)-OH
The primary amine can be covalently coupled with N-hydroxysuccinimide (NHS) activated esters to form stable amide bonds
C15H27N3O11 / 425
6-(2-Acetamido-2-deoxy-β-D-Galactopyranosyl-oxy) hexanoic acid
/ IgA1(222-240)-Tn(228
GA531005: Fmoc-Thr(Glc(Ac)4-α-D)-OH Pack Size:250 mg Fmoc-Ser(β-D-GlcNAc(Ac)3-(1-3)-α-D-GalNAc(Ac)2)-OHC33H37NO14 671. 65 An Fmoc protected L threonine 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
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