[H]\C(=C(/[H])C1=CC=CC=C1)C(=O)O[C@]1([H])[C@@]([H])(O)[C@]([H])(O)[C@@]([H])(CO)O[C@@]1([H])C1=C(OC)C=C(C)C2=C1OC(=CC2=O)[C@]([H])(O)[C@]([H])(C)O

InChIKey=HLFYJFSIVFUDFJ-XUBKHSKJSA-N

C29H32O11

556.564

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Cinnamic acid esters C-glycosyl compounds Chromones Styrenes Anisoles Alkyl aryl ethers Pyranones and derivatives Fatty acid esters Oxanes Monosaccharides Enoate esters Heteroaromatic compounds Secondary alcohols Dialkyl ethers Monocarboxylic acids and derivatives Oxacyclic compounds Organic oxides Carbonyl compounds Aromatic alcohols Hydrocarbon derivatives Primary alcohols

Aromatic heteropolycyclic compounds

Phenolic glycoside - Cinnamic acid or derivatives - Cinnamic acid ester - Chromone - C-glycosyl compound - Benzopyran - 1-benzopyran - Anisole - Styrene - Alkyl aryl ether - Fatty acid ester - Pyranone - Monosaccharide - Oxane - Monocyclic benzene moiety - Benzenoid - Pyran - Fatty acyl - Heteroaromatic compound - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Secondary alcohol - Dialkyl ether - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Ether - Monocarboxylic acid or derivatives - Primary alcohol - Organic oxide - Alcohol - Carbonyl group - Aromatic alcohol - Hydrocarbon derivative - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Not available