CC(=O)NC1=C(Cl)C=CC(CO[C@@H]2O[C@H](CNC(=O)CC3=CC=CC=C3)[C@@H](O[C@H]3O[C@@H]4COC(O[C@H]4[C@H](O)[C@H]3O)C3=CC=CC=C3)[C@H](O)[C@H]2O)=C1

InChIKey=YUGFUUXMJPCPBS-LYSUMFSHSA-N

C36H41ClN2O12

729.18

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

O-glycosyl compounds

O-haloacetanilides Disaccharides Pyranodioxins Phenylacetamides N-acetylarylamines Chlorobenzenes Oxanes 1,3-dioxanes Aryl chlorides Acetamides Secondary carboxylic acid amides Secondary alcohols Oxacyclic compounds Acetals Carbonyl compounds Organochlorides Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

O-haloacetanilide - Haloacetanilide - Disaccharide - O-glycosyl compound - Acetanilide - Pyranodioxin - Phenylacetamide - N-acetylarylamine - Anilide - N-arylamide - Chlorobenzene - Halobenzene - Meta-dioxane - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Oxane - Benzenoid - Acetamide - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Carboxylic acid derivative - Acetal - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic nitrogen compound - Alcohol - Organonitrogen compound - Organohalogen compound - Organochloride - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Not available