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C100H159N23O39S / 2339
O-glucosylation of Ser is a known modification of EGF-like domains
81 / An Fmoc-protected lysine glycation building block for solid-phase peptide synthesis (SPPS)
(Xylα(1-4)GlcA)-β-O-4-MU
Tumour-associated carbohydrate antigen (TACA)
GA631005: Fmoc-Thr(α-D-Man(Ac)4-(1-2)α-D-Man(Ac)3)-OH Pack Size:100 mg C100H159N23O39S / 2339C45H53NO22 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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