CC[N+]1=C(SC2=CC=CC=C12)\C=C\C1=CC=C(O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)C=C1

InChIKey=ORJJFHPLGOUFQQ-IMEYOLAUSA-N

C23H26NO6S

444.52

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Benzothiazoles Styrenes Phenol ethers Phenoxy compounds Oxanes Heteroaromatic compounds Thiazoles Secondary alcohols Azacyclic compounds Oxacyclic compounds Acetals Polyols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Primary alcohols Organic cations

Aromatic heteropolycyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - 1,3-benzothiazole - Phenoxy compound - Styrene - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Oxane - Azole - Heteroaromatic compound - Thiazole - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Alcohol - Primary alcohol - Organic cation - 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