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N-α-Fmoc-N-γ-(2-acetamido-2-deoxy-3
C62H98N16O28 / 1515
O-glycosylation (α-GalNAc) at Ser1183
C38H50N2O11 / 710
N-α-Fmoc-O-β-[2-acetamido-2-deoxy-4-O-(3
GA631005: Fmoc-Thr(α-D-Man(Ac)4-(1-2)α-D-Man(Ac)3)-OH Pack Size:100 mg N-α-Fmoc-N-γ-(2-acetamido-2-deoxy-3C45H53NO22 959. 9 An Fmoc protected L threonine building block carrying a Man1 2Man disaccharide, 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 acetate esters (peracetate), which keep the glycan inert
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