CN(C)CCN1C(=O)C2=CC=CC3=CC(NCC4=CC=CC=C4O[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=CC(C1=O)=C23

InChIKey=XZBXZYYJNXXRLF-VMQCTCBBSA-N

C29H33N3O8

551.596

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses Isoquinolones and derivatives O-glycosyl compounds Naphthalenes Benzylamines Phenol ethers Phenoxy compounds Phenylmethylamines Secondary alkylarylamines Aralkylamines Oxanes N-substituted carboxylic acid imides Secondary alcohols Trialkylamines Amino acids and derivatives Oxacyclic compounds Acetals Azacyclic compounds Polyols Organopnictogen compounds Organic oxides Primary alcohols Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenolic glycoside - Hexose monosaccharide - Isoquinolone - O-glycosyl compound - Naphthalene - Benzylamine - Phenoxy compound - Phenol ether - Phenylmethylamine - Aralkylamine - Secondary aliphatic/aromatic amine - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Carboxylic acid imide, n-substituted - Oxane - Carboxylic acid imide - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Acetal - Carboxylic acid derivative - Polyol - Primary alcohol - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - Amine - Organopnictogen compound - Organic oxide - Organonitrogen compound - 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