OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@@H](OC3=CC=C(C=C3)[N+]([O-])=O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey=IAYJZWFYUSNIPN-LTHBGAKLSA-N

C18H25NO13

463.392

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glycosyl compounds Disaccharides Nitrobenzenes Phenoxy compounds Phenol ethers Nitroaromatic compounds Oxanes Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Polyols Oxacyclic compounds Organic oxoazanium compounds Acetals Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - O-glycosyl compound - Disaccharide - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Benzenoid - Oxane - Monocyclic benzene moiety - Organic nitro compound - Secondary alcohol - C-nitro compound - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Polyol - Organic oxoazanium - Acetal - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Primary alcohol - Organonitrogen compound - 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