72601-82-2

Basic information

• Product Name: 4-METHYLUMBELLIFERYL BETA-L-FUCOPYRANOSIDE
• Synonyms: METHYLUMBELLIFERYL-B-L-FUCOPYRANOSIDE, 4-;4-METHYLUMBELLIFERYL BETA-L-FUCOPYRANOSIDE;4-METHYLUMBELLIFERYL BETA-L-FUCOSIDE;4-MU-BETA-L-FUC;4-methylumbelliferyl-B-L-fucoside;7-[(6-deoxy-beta-L-galactopyranosyl)oxy]-4-methyl-2H-1-benzopyran-2-one;4-Methylumbelliferyl-B-LFuco-;4-Methylumbelliferylb-L-fucopyranoside
• CAS NO: 72601-82-2
• Molecular Formula: C16H18O7
• Molecular Weight: 322.31
• EINECS: 276-730-0
• Product Categories: Substrates;substrate
• Mol File: 72601-82-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 565.9 °C at 760 mmHg
• Flash Point: 211.3 °C
• Appearance: /
• Density: 1.441 g/cm³
• Vapor Pressure: 1.21E-13mmHg at 25°C
• Refractive Index: 1.621
• Storage Temp.: −20°C
• Solubility: DMSO (Slightly)
• CAS DataBase Reference: 4-METHYLUMBELLIFERYL BETA-L-FUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYLUMBELLIFERYL BETA-L-FUCOPYRANOSIDE(72601-82-2)
• EPA Substance Registry System: 4-METHYLUMBELLIFERYL BETA-L-FUCOPYRANOSIDE(72601-82-2)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 72601-82-2(Hazardous Substances Data)

Usage

Chemical Properties

solid

InChI:InChI=1/C16H18O7/c1-7-5-12(17)23-11-6-9(3-4-10(7)11)22-16-15(20)14(19)13(18)8(2)21-16/h3-6,8,13-16,18-20H,1-2H3/t8-,13+,14+,15-,16+/m0/s1

Upstream product

• 16741-27-8 2,3,4-tri-O-acetyl-α-L-fucopyranosyl bromide 
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• 7404-35-5 1,2,3,4-tetra-O-acetyl-L-rhamnopyranose 
• 28915-80-2 2,3,4-tri-O-acetyl-L-rhamnopyranose 
• 122089-71-8 2,3,4-tri-O-acetyl-L-rhamnopyranosyl trichloroacetimidate 

Relevant articles and documents

CARBONIC ANHYDRASE INHIBITORS WITH ANTIMETASTATIC ACTIVITY

Compositions for the treatment of cancer comprising coumarin and thiocoumarin derivatives of Formulas I- XII are disclosed. Said derivatives preferentially inhibit carbonic anhydrase IX and XII (which are associated with hypoxic and metastatic tumours) over inhibiting carbonic anhydrase I and II activity. The compositions therefore are suited for treatment of hypoxic or metastatic cancers due to this selective mechanism of action.

Profiling of glycosidase activities using coumarin-conjugated glycoside cocktails

Glycosidases are a large subgroup of carbohydrate-processing enzymes that hydrolytically cleave the glycosidic bond. Glycans formed by the action of glycosidases are involved in various biological processes. Genetic abnormalities in glycosidases are associated with inherited diseases. Thus, characterization of the catalytic activities of glycosidases is of great importance. Herein, we describe a simple and rapid approach for determining glycosidase activity profiles using coumarin-conjugated glycoside cocktails.