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p-Nitrophenyl α-D-mannopyranoside

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Biochemical Assay Reagents (2) Glycosidase (1)

Inhibitors & Agonists

Biochemical Assay Reagents

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-137822

**p-Nitrophenyl α-D-mannopyranoside** 4-Nitrophenyl a-D-mannopyranoside	Glycosidase	Others
p-Nitrophenyl α-D-mannopyranoside (4-Nitrophenyl α-D-mannopyranoside) is a chromogenic glycosidic ligand. p-Nitrophenyl α-D-mannopyranoside features a sugar moiety (α-D-mannopyranose) with the mannose-characteristic axial hydroxyl group at the C2 position and a ligand portion (p-nitrophenol) that provides ultraviolet-visible light absorption properties. p-Nitrophenyl α-D-mannopyranoside can be used to determine glycosidase activity and characterize the sugar recognition properties of lectins (such as Concanavalin A (HY-P2149)) .

HY-W776875

**p-Nitrophenyl 3-O-α-D-mannopyranosyl-α-D-mannopyranoside**	Biochemical Assay Reagents	Others
p-Nitrophenyl 3-O-α-D-mannopyranosyl-α-D-mannopyranoside is a biochemical assay reagent.

HY-W396250

**p-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside**	Biochemical Assay Reagents	Others
p-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology .

Cat. No.	Product Name	Type

HY-137822

**p-Nitrophenyl α-D-mannopyranoside** 4-Nitrophenyl a-D-mannopyranoside	Carbohydrates
p-Nitrophenyl α-D-mannopyranoside (4-Nitrophenyl α-D-mannopyranoside) is a chromogenic glycosidic ligand. p-Nitrophenyl α-D-mannopyranoside features a sugar moiety (α-D-mannopyranose) with the mannose-characteristic axial hydroxyl group at the C2 position and a ligand portion (p-nitrophenol) that provides ultraviolet-visible light absorption properties. p-Nitrophenyl α-D-mannopyranoside can be used to determine glycosidase activity and characterize the sugar recognition properties of lectins (such as Concanavalin A (HY-P2149)) .

p-Nitrophenyl α-D-mannopyranoside

4-Nitrophenyl a-D-mannopyranoside

Carbohydrates

p-Nitrophenyl α-D-mannopyranoside (4-Nitrophenyl α-D-mannopyranoside) is a chromogenic glycosidic ligand. p-Nitrophenyl α-D-mannopyranoside features a sugar moiety (α-D-mannopyranose) with the mannose-characteristic axial hydroxyl group at the C2 position and a ligand portion (p-nitrophenol) that provides ultraviolet-visible light absorption properties. p-Nitrophenyl α-D-mannopyranoside can be used to determine glycosidase activity and characterize the sugar recognition properties of lectins (such as Concanavalin A (HY-P2149)) .

HY-W776875

**p-Nitrophenyl 3-O-α-D-mannopyranosyl-α-D-mannopyranoside**	Carbohydrates
p-Nitrophenyl 3-O-α-D-mannopyranosyl-α-D-mannopyranoside is a biochemical assay reagent.

HY-W396250

**p-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside**	Carbohydrates
p-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology .

p-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside

Carbohydrates

p-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology .

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