OC[C@H](NC(=O)C1=C2O[Fe+]OC2=CC(=C1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C([O-])=O

InChIKey=XQDCQPPMOATTGF-CSCLAODDSA-K

C16H18FeNO11

456.161

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

N-acyl-alpha amino acids Serine and derivatives Hexoses C-glycosyl compounds Beta hydroxy acids and derivatives Oxanes Benzenoids Secondary carboxylic acid amides Secondary alcohols Carboxylic acid salts Polyols Oxacyclic compounds Organic transition metal salts Monocarboxylic acids and derivatives Metalloheterocyclic compounds Dialkyl ethers Carboxylic acids Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Phenolic glycoside - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - Serine or derivatives - Hexose monosaccharide - C-glycosyl compound - Alpha-amino acid or derivatives - Beta-hydroxy acid - Benzenoid - Oxane - Monosaccharide - Hydroxy acid - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid salt - Carboxamide group - Oxacycle - Organic metal salt - Organic transition metal salt - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Metalloheterocycle - Ether - Dialkyl ether - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organic zwitterion - Primary alcohol - Organonitrogen compound - Carbonyl group - Alcohol - 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