CCCCCc1cc(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)c2[C@@H]3C=C(CO)CC[C@H]3C(C)(C)Oc2c1

InChIKey=YVVTYNYUWOSVJS-RNRFLGCGSA-N

C27H38O9

506.592

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides 2,2-dimethyl-1-benzopyrans Hexoses O-glycosyl compounds Alkyl aryl ethers Beta hydroxy acids and derivatives Pyrans Oxanes Benzenoids Secondary alcohols Acetals Polyols Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Carbonyl compounds Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Hexose monosaccharide - 2,2-dimethyl-1-benzopyran - O-glycosyl compound - Chromane - Benzopyran - 1-benzopyran - Alkyl aryl ether - Beta-hydroxy acid - Oxane - Benzenoid - Monosaccharide - Hydroxy acid - Pyran - Secondary alcohol - Polyol - Organoheterocyclic compound - Oxacycle - Monocarboxylic acid or derivatives - Ether - Carboxylic acid - Carboxylic acid derivative - Acetal - Primary alcohol - Alcohol - Carbonyl group - Organic oxide - 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