CCC1=CC=C(CC2=C(C)C(O[C@H]3CCOC3)=CC(=C2)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1

InChIKey=UBKUPNNSSRHNCZ-ZWQPWAMFSA-N

C26H34O7

458.551

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Diphenylmethanes C-glycosyl compounds Phenoxy compounds Phenol ethers Toluenes Alkyl aryl ethers Oxanes Monosaccharides Oxolanes Secondary alcohols 1,2-diols Oxacyclic compounds Dialkyl ethers Primary alcohols Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Diphenylmethane - C-glycosyl compound - Phenoxy compound - Phenol ether - Alkyl aryl ether - Toluene - Oxane - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Oxolane - Secondary alcohol - 1,2-diol - Polyol - Organoheterocyclic compound - Ether - Oxacycle - Dialkyl ether - Primary alcohol - Hydrocarbon derivative - Alcohol - 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