OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)C1=CC=CC(=C1)C1=CC=C(C=C1)[C@@H]1[C@@H](CC[C@H](O)C2=CC=C(F)C=C2)C(=O)N1C1=CC=CC=C1

InChIKey=WMMBKQAHXBYLLA-OMGMQEPBSA-N

C36H36FNO7

613.682

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Monobactams Biphenyls and derivatives Hexoses C-glycosyl compounds Phenylazetidines Fluorobenzenes Aryl fluorides Oxanes Tertiary carboxylic acid amides Secondary alcohols Polyols Dialkyl ethers Azacyclic compounds Oxacyclic compounds Organofluorides Organic oxides Aromatic alcohols Hydrocarbon derivatives Primary alcohols Carbonyl compounds Organonitrogen compounds

Aromatic heteromonocyclic compounds

Phenolic glycoside - Monobactam - Hexose monosaccharide - Biphenyl - C-glycosyl compound - 1-phenylazetidine - 2-phenylazetidine - Halobenzene - Fluorobenzene - Monosaccharide - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Oxane - Benzenoid - Tertiary carboxylic acid amide - Beta-lactam - Azetidine - Carboxamide group - Secondary alcohol - Lactam - Polyol - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Carboxylic acid derivative - Organofluoride - Carbonyl group - Aromatic alcohol - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Alcohol - Organic oxide - Organonitrogen compound - Organohalogen 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