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4-Nitrophenyl (pNP) glycosides are chromogenic enzyme substrates: cleavage of the glycosidic bond by the target enzyme releases free 4-nitrophenol
4-Carboxybutyl β-D-glucopyranoside
or pentafluorophenyl (PFP) esters and reacted with amine-functionalized platforms or lysine residues on proteins and peptides to form stable amide bonds
49 / / Estrone-O-β-D-Glucuronide / Estrone Glucuronide
6-(4-{1-(4-Fluoro-phenyl)-3-[3-(4-fluoro-phenyl)-3-hydroxy-propyl]-4-oxo-azetidin-2-yl}-phenoxy)-3
AG624000: α-D-Man-Ethyl-Azide Pack Size:1 g 4-Nitrophenyl (pNP) glycosides are chromogenicC8H15N3O6 249. 22 An D mannose ligand equipped with an azide functionalized linker through a short ethyl spacer. The terminal azide can be covalently coupled to alkyne partners via copper catalyzed azide alkyne cycloaddition (CuAAC), or to dibenzocyclooctyne (DBCO) and related strained alkynes using copper free click chemistry, forming stable 1,2,3 triazole linkages. This compound provides an D mannose building block for glycoconjugate synthesis and
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