CAS 383160-16-5
:4-methyl-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-[[(2R,4S,5S)-3,4,5-trihydroxy-6-[[(2R,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-2-one
Description:
The chemical substance known as 4-methyl-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-[[(2R,4S,5S)-3,4,5-trihydroxy-6-[[(2R,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-2-one, with the CAS number 383160-16-5, is a complex organic compound characterized by its chromone backbone and multiple hydroxyl groups. This structure suggests it may exhibit significant biological activity, potentially acting as a flavonoid or polyphenolic compound. The presence of multiple tetrahydropyran rings indicates a high degree of stereochemistry, which can influence its solubility, reactivity, and interaction with biological targets. Such compounds are often studied for their antioxidant properties, potential therapeutic effects, and roles in various biochemical pathways. The intricate arrangement of hydroxyl groups may enhance its ability to form hydrogen bonds, affecting its pharmacokinetics and bioavailability. Overall, this compound exemplifies the complexity and diversity of natural products in medicinal chemistry.
Formula:C28H38O18
InChI:InChI=1/C28H38O18/c1-9-4-16(30)43-12-5-10(2-3-11(9)12)42-28-25(39)22(36)19(33)15(46-28)8-41-27-24(38)21(35)18(32)14(45-27)7-40-26-23(37)20(34)17(31)13(6-29)44-26/h2-5,13-15,17-29,31-39H,6-8H2,1H3/t13?,14?,15?,17-,18-,19-,20+,21+,22+,23?,24?,25?,26-,27-,28-/m1/s1
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Found 3 products.
4-Methylumbelliferyl β-D-Gentotrioside
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications 4-Methylumbelliferyl β-D-Gentotrioside (cas# 383160-16-5) is a compound useful in organic synthesis.<br></p>Formula:C28H38O18Color and Shape:NeatMolecular weight:662.594-Methylumbelliferyl b-D-gentiotrioside
CAS:<p>4-Methylumbelliferyl beta-D-gentiotrioside is a fluorogenic substrate for beta-glucosidase. 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 beta-D-gentiotriosideas a substrate for measuring the beta-glucosidase activity is used for Gaucher disease screening.</p>Formula:C28H38O18Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:662.59 g/mol


