10357-27-4
10357-27-4
Chemical Structure
p-Nitrophenyl α-D-mannopyranoside
Synonym(s): 4-Nitrophenyl a-D-mannopyranoside
- CAS. Nr.: 10357-27-4
- Formula:C12H15NO8
- Molecular Weight:301.25
IUPAC Name: (2R,3S,4S,5S,6R)-2-(hydroxymethyl)-6-(4-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: IFBHRQDFSNCLOZ-GCHJQGSQSA-N
SMILES: O[C@@H]([C@H]([C@@H]1O)O)[C@H](O[C@@H]1CO)OC(C=C2)=CC=C2[N](=O)=O
Biological Activity: 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))[1][2].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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p-Nitrophenyl α-D-mannopyranoside | 98.88% | 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)). | ||||||||||||||||||||
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4-Nitrophenyl α-L-arabinofuranoside | 4-Nitrophenyl α-L-arabinofuranoside is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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p-Nitrophenyl α-L-fucoside | 98.80% | p-Nitrophenyl α-L-fucoside (PNP α-L-Fuc) is a specific substrate of Pecten maximus α-L-fucosidase, with a Km value of 650 µM. p-Nitrophenyl α-L-fucoside serves as a substrate for ClAgl29A and ClAgl29B. Enzymatic hydrolysis of p-Nitrophenyl α-L-fucoside releases p-nitrophenol and α-L-fucose, where the latter undergoes mutarotation over time to form β-L-fucose. p-Nitrophenyl α-L-fucoside is not the preferred substrate for ClAgl29A and ClAgl29B. | ||||||||||||||||||||
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4-Nitrophenyl β-D-fucopyranoside | 4-Nitrophenyl β-D-fuco-pyran-oside is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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4-Nitrophenyl β-D-galactopyranoside | 99.39% | 4-Nitrophenyl β-D-galactopyranoside is a derivative of beta-D-galactoside and monosaccharide. 4-Nitrophenyl β-D-galactopyranoside can be used for affinity label. | ||||||||||||||||||||
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4-Nitrophenyl α-L-rhamnopyranoside | 99.83% | 4-Nitrophenyl α-L-rhamnopyranoside is a commonly used substrate in various biochemical assays to measure the activity of enzymes that hydrolyze rhamnose, such as α-L-rhamnosidase. 4-Nitrophenyl α-L-rhamnopyranoside has unique chemical properties that allow it to be hydrolyzed by these enzymes to form a yellow product called p-nitrophenol. This makes it a useful tool for detecting and quantifying rhamnohydrolase activity in biological samples or microbial cultures. | ||||||||||||||||||||
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4-Nitrophenyl β-D-glucopyranoside | 99.77% | 4-Nitrophenyl β-D-glucopyranoside is a chromogenic substrate for β-glucosidase. 4-Nitrophenyl β-D-glucopyranoside is converted to a colored product, p-nitrophenol that is easily detected spectrophotometrically at 405 nm when used in a β-glycosidase assay. 4-Nitrophenyl β-D-glucopyranoside is hydrolysed through intramolecular nucleophilic catalysis by the phosphate group in the 2-position. 4-Nitrophenyl β-D-glucopyranoside is promising for research of postmenopausal osteoporosis. | ||||||||||||||||||||
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4-Nitrophenyl β-D-mannopyranoside | 98.50% | 4-Nitrophenyl β-D-mannopyranoside is a useful substrate for β-D-mannopyranosidase. 4-Nitrophenyl β-D-mannopyranoside is also a substrate for GH1-glucosidase (EaBgl1A) and α-L-rhamnosidase. | ||||||||||||||||||||
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4-Nitrophenyl a-D-glucopyranoside | 99.78% | 4-Nitrophenyl a-D-glucopyranoside is a chromogenic substrate for α-glucosidase. 4-Nitrophenyl a-D-glucopyranoside can be used to measure of α-glucosidase activity. | ||||||||||||||||||||
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4-Nitrophenyl α-D-galactopyranoside | 98.70% | 4-Nitrophenyl α-D-galactopyranoside (PNP-alpha-D-Gal) is an artificial substrate of 4-nitrophenyl (pNP) glycopyranoside for detecting α-galactosidase activity. The amount of released pNP is significantly increased when 4-Nitrophenyl α-D-galactopyranoside is used as substrates. | ||||||||||||||||||||
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4-Nitrophenyl β-L-fucopyranoside | 4-Nitrophenyl β-L-fucopyranoside is a biochemical reagent. | |||||||||||||||||||||
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