CN(C)C1=CC=C(C=C1)C#C\C=C\C1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C(C=C1)[N+]([O-])=O

InChIKey=YEPBHANWHHAEFU-BQGJUYRASA-N

C24H26N2O8

470.478

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Nitrobenzenes Aniline and substituted anilines Dialkylarylamines Styrenes Nitroaromatic compounds Phenol ethers Phenoxy compounds Oxanes Secondary alcohols Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Acetals Polyols Organopnictogen compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives Primary alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Styrene - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Oxane - Organic nitro compound - Tertiary amine - Secondary alcohol - C-nitro compound - Organoheterocyclic compound - Oxacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Polyol - Acetal - Organic oxoazanium - Organic oxide - Organonitrogen compound - Alcohol - Amine - Primary alcohol - Organic nitrogen compound - Organic zwitterion - Organic salt - Hydrocarbon derivative - 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