OC[C@@H]1O[C@@H](OC2=CC(=CC(=C2)C(=O)CCCCC(=O)C2=CC(O[C@@H]3O[C@@H](CO)[C@H](O)[C@@H](O)[C@H]3O)=CC(=C2)C2=CC(CC(O)=O)=CC=C2)C2=CC(CC(O)=O)=CC=C2)[C@H](O)[C@H](O)[C@H]1O

InChIKey=JNJMLTWWOCMPRL-XJBNHSCKSA-N

C46H50O18

890.888

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Alkyl-phenylketones Biphenyls and derivatives Butyrophenones O-glycosyl compounds Aryl alkyl ketones Benzoyl derivatives Phenoxy compounds Phenol ethers Monosaccharides Dicarboxylic acids and derivatives Oxanes Secondary alcohols Carboxylic acids Polyols Oxacyclic compounds Acetals Hydrocarbon derivatives Primary alcohols Aldehydes Organic oxides

Aromatic heteromonocyclic compounds

Phenolic glycoside - Alkyl-phenylketone - Biphenyl - Butyrophenone - O-glycosyl compound - Phenylketone - Benzoyl - Phenoxy compound - Phenol ether - Aryl ketone - Aryl alkyl ketone - Monocyclic benzene moiety - Benzenoid - Dicarboxylic acid or derivatives - Oxane - Monosaccharide - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Carboxylic acid derivative - Carboxylic acid - Alcohol - Organic oxide - Carbonyl group - Primary alcohol - Aldehyde - Hydrocarbon derivative - Aromatic heteromonocyclic 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