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Results for "

α-D-mannopyranose

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Bacterial (1) Biochemical Assay Reagents (9) Environmental Pollutants (1) Glycosidase (1) Lactate Dehydrogenase (1)
By Research Areas:	Infection (1) Metabolic Disease (1)
Click Chemistry:	Azide (1)

Inhibitors & Agonists

Biochemical Assay Reagents

Click Chemistry

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-W039897

Methyl α-D-mannopyranoside 1 Publications Verification α-Methyl-D-mannoside	Environmental Pollutants Bacterial	Infection
Methyl α-D-mannopyranoside (α-Methyl-D-mannoside) is a methyl glycoside derivative and conformational stabilizer of α-D-mannopyranose. The glycosidic bond conformation of Methyl α-D-mannopyranoside is significantly affected by the environment. In aqueous solution, Methyl α-D-mannopyranoside stabilizes into a trans conformation via intermolecular hydrogen bonds; in the gas phase, however, steric interactions drive Methyl α-D-mannopyranoside to prefer a clockwise gauche conformation. Methyl α-D-mannopyranoside also serves as a major component of secondary cell wall polymers in some bacteria and an active precursor site for virus-targeted glycoproteins. Methyl α-D-mannopyranoside acts as an acceptor substrate for alternansucrase, mediating the transfer of D-glucopyranosyl groups to generate a variety of glycosylated oligosaccharide products, with methyl α-D-glucopyranosyl-(1→6)-α-D-mannopyranoside as the main component. Methyl α-D-mannopyranoside is applicable to studies on bacterial pathogenic mechanisms associated with mannose-specific fimbrial lectins .

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-W039898

α-D-Mannose pentaacetate 1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose	Biochemical Assay Reagents Lactate Dehydrogenase	Metabolic Disease
α-D-Mannose pentaacetate (1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose) acts as a lactate promoter. It increases lactate production in rat red blood cells .

HY-W145616

1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose	Biochemical Assay Reagents	Others
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

HY-W699112

α-D-Mannopyranose,1,2,3,6-tetrabenzoate	Biochemical Assay Reagents	Others
α-D-Mannopyranose,1,2,3,6-tetrabenzoate 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 .

HY-W416016

3-O-(Phenylmethyl)-α-D-mannopyranose	Biochemical Assay Reagents	Others
3-O-(Phenylmethyl)-α-D-mannopyranose 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 .

HY-W412469

α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate	Biochemical Assay Reagents	Others
α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate 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 .

HY-W145614

1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose	Biochemical Assay Reagents	Others
1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-W779201

2,3:4,6-Di-O-cyclohexylidene-α-D-mannopyranose	Biochemical Assay Reagents	Others
2,3:4,6-Di-O-cyclohexylidene-α-D-mannopyranose 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 .

HY-W776829

2,3-O-Carbonyl-1,4,6-tri-O-acetyl-α-D-mannopyranose	Biochemical Assay Reagents	Others
2,3-O-Carbonyl-1,4,6-tri-O-acetyl-α-D-mannopyranose 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 .

HY-W145700

2-O-Benzyl-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose 1,3,4,6-Tetra-O-acetyl-2-O-benzyl-a-D-mannopyranose	Biochemical Assay Reagents	Others
2-O-Benzyl-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Cat. No.	Product Name	Type

HY-137822

p-Nitrophenyl α-D-mannopyranoside 4-Nitrophenyl a-D-mannopyranoside	Biochemical Assay Reagents
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

Biochemical Assay Reagents

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-W039898

α-D-Mannose pentaacetate 1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose	Biochemical Assay Reagents
α-D-Mannose pentaacetate (1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose) acts as a lactate promoter. It increases lactate production in rat red blood cells .

HY-W699112

α-D-Mannopyranose,1,2,3,6-tetrabenzoate	Biochemical Assay Reagents
α-D-Mannopyranose,1,2,3,6-tetrabenzoate 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 .

α-D-Mannopyranose,1,2,3,6-tetrabenzoate

Biochemical Assay Reagents

α-D-Mannopyranose,1,2,3,6-tetrabenzoate 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 .

HY-W416016

3-O-(Phenylmethyl)-α-D-mannopyranose	Biochemical Assay Reagents
3-O-(Phenylmethyl)-α-D-mannopyranose 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 .

3-O-(Phenylmethyl)-α-D-mannopyranose

Biochemical Assay Reagents

3-O-(Phenylmethyl)-α-D-mannopyranose 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 .

HY-W412469

α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate	Biochemical Assay Reagents
α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate 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 .

α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate

Biochemical Assay Reagents

α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate 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 .

HY-W145614

1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose	Biochemical Assay Reagents
1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranose is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-W779201

2,3:4,6-Di-O-cyclohexylidene-α-D-mannopyranose	Biochemical Assay Reagents
2,3:4,6-Di-O-cyclohexylidene-α-D-mannopyranose 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 .

2,3:4,6-Di-O-cyclohexylidene-α-D-mannopyranose

Biochemical Assay Reagents

2,3:4,6-Di-O-cyclohexylidene-α-D-mannopyranose 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 .

HY-W776829

2,3-O-Carbonyl-1,4,6-tri-O-acetyl-α-D-mannopyranose	Biochemical Assay Reagents
2,3-O-Carbonyl-1,4,6-tri-O-acetyl-α-D-mannopyranose 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 .

2,3-O-Carbonyl-1,4,6-tri-O-acetyl-α-D-mannopyranose

Biochemical Assay Reagents

2,3-O-Carbonyl-1,4,6-tri-O-acetyl-α-D-mannopyranose 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 .

HY-W145700

2-O-Benzyl-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose 1,3,4,6-Tetra-O-acetyl-2-O-benzyl-a-D-mannopyranose	Biochemical Assay Reagents
2-O-Benzyl-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Cat. No.	Product Name		Classification

HY-W145616

1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose		Azide
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

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