OC[C@@]1(O)CO[C@@H](OC[C@H]2O[C@@H](Oc3ccc(CC[N+]([O-])=O)cc3)[C@H](O)[C@@H](O)[C@@H]2O)[C@@H]1O

InChIKey=GVFCXNBFDQOBRP-OTCFHACESA-N

C19H27NO12

461.42

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

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

Aromatic heteromonocyclic compounds

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