CC1=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(CC2=NC=CO2)=CC=C1

InChIKey=LOFSDOBCMNTTLT-AQFIFQLPSA-N

C17H21NO7

351.355

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glycosyl compounds Phenol ethers Phenoxy compounds Toluenes Monosaccharides Oxanes Oxazoles Heteroaromatic compounds Secondary alcohols Azacyclic compounds Oxacyclic compounds Acetals Polyols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Primary alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - O-glycosyl compound - Phenoxy compound - Phenol ether - Toluene - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Azole - Heteroaromatic compound - Oxazole - Secondary alcohol - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Alcohol - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Primary alcohol - Organopnictogen compound - 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