NCCOC1=CC(Cl)=C(CC2=CC3=CC=CC=C3S2)C=C1[C@@H]1O[C@H](COCC2=CC=CC=C2)[C@@H](OCC2=CC=CC=C2)[C@H](OCC2=CC=CC=C2)[C@H]1OCC1=CC=CC=C1

InChIKey=VZMJLTVYZKYPNF-XGPTVIORSA-N

C51H50ClNO6S

840.47

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses C-glycosyl compounds 1-benzothiophenes Benzylethers Phenoxy compounds Phenol ethers 2,3,5-trisubstituted thiophenes Alkyl aryl ethers Chlorobenzenes Oxanes Aryl chlorides Heteroaromatic compounds Oxacyclic compounds Dialkyl ethers Hydrocarbon derivatives Monoalkylamines Organochlorides

Aromatic heteropolycyclic compounds

Phenolic glycoside - Hexose monosaccharide - C-glycosyl compound - 1-benzothiophene - Benzothiophene - Benzylether - Phenoxy compound - 2,3,5-trisubstituted thiophene - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Oxane - Thiophene - Heteroaromatic compound - Ether - Dialkyl ether - Organoheterocyclic compound - Oxacycle - Primary aliphatic amine - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organohalogen compound - Organochloride - Organonitrogen compound - Primary amine - 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