CAS 383160-15-4
:7-[[4-O-(6-Deoxy-α-L-galactopyranosyl)-β-D-galactopyranosyl]oxy]-4-methyl-2H-1-benzopyran-2-one
Description:
The chemical substance known as "7-[[4-O-(6-Deoxy-α-L-galactopyranosyl)-β-D-galactopyranosyl]oxy]-4-methyl-2H-1-benzopyran-2-one," with the CAS number 383160-15-4, is a flavonoid glycoside. This compound features a benzopyran backbone, which is characteristic of flavonoids, and is substituted with multiple sugar moieties, specifically a 6-deoxy-α-L-galactopyranosyl group and a β-D-galactopyranosyl group. These sugar attachments enhance its solubility and bioactivity. The presence of the methyl group at the 4-position of the benzopyran ring contributes to its structural diversity and potential biological activity. Flavonoid glycosides are known for their antioxidant properties and may exhibit various pharmacological effects, including anti-inflammatory and antimicrobial activities. The specific arrangement of the sugar units and the benzopyran structure may influence its interaction with biological systems, making it a subject of interest in medicinal chemistry and natural product research. Further studies would be necessary to elucidate its precise biological functions and potential applications.
Formula:C22H28O12
InChI:InChI=1S/C22H28O12/c1-8-5-14(24)32-12-6-10(3-4-11(8)12)31-22-19(29)17(27)20(13(7-23)33-22)34-21-18(28)16(26)15(25)9(2)30-21/h3-6,9,13,15-23,25-29H,7H2,1-2H3/t9-,13+,15+,16+,17+,18-,19+,20-,21-,22+/m0/s1
InChI key:InChIKey=UAKRUHKRXFCMAA-UGFGAIGFSA-N
SMILES:CC=1C=2C(=CC(O[C@@H]3O[C@H](CO)[C@H](O[C@H]4[C@@H](O)[C@H](O)[C@H](O)[C@H](C)O4)[C@H](O)[C@H]3O)=CC2)OC(=O)C1
Synonyms:- 7-[[4-O-(6-Deoxy-α-L-galactopyranosyl)-β-D-galactopyranosyl]oxy]-4-methyl-2H-1-benzopyran-2-one
- 2H-1-Benzopyran-2-one, 7-[[4-O-(6-deoxy-α-L-galactopyranosyl)-β-D-galactopyranosyl]oxy]-4-methyl-
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Found 2 products.
4-Methylumbelliferyl 4-O-(α-L-fucopyranosyl)-β-D-galactopyranoside
CAS:4-Methylumbelliferyl 4-O-(alpha-L-fucopyranosyl)-beta-D-galactopyranoside is a fluorogenic substrate for alpha-L-fucosidase. After enzymatic cleaveage, free 4-methylumbelliferone (also known as hymecromone) is released, exhibiting blue fluorescence upon excitation with UV light. The strongest fluorescence of 4-methylumbelliferone requires deprotonation of the hydroxyl group (thus requires alkaline pH), with a maximal fluorescence intensity obtained with excitation at 350 to 370 nm and emission at 440 to 470 nm. The use of 4-methylumbelliferyl 4-O-(alpha-L-fucopyranosyl)-beta-D-galactopyranosideas a substrate for measuring the alpha-L-fucosidase activity is used for fucosidosis diagnosis and in screening studies of glycoprotein metabolism disorders.Formula:C22H28O12Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:484.45 g/mol

