Compound Identification
SMILES
CC1=CC(C(=O)C2=CC=CC=C2C)=C(O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)C=C1
InChIKey
InChIKey=DIJILNYBBGBSNM-NMLACTOBSA-N
Formula
C20H22O6
Mass
358.39
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Level 5
Glycosyl compounds
- Level 6 Phenolic glycosides
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Level 5
Glycosyl compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Class
Organooxygen compounds
-
Superclass
Organic oxygen compounds
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Glycosyl compounds
Direct Parent
Phenolic glycosides
Alternative Parents
Benzophenones Aryl-phenylketones Diphenylmethanes O-glycosyl compounds Pentoses Benzoyl derivatives Phenoxy compounds Phenol ethers Toluenes Oxanes Secondary alcohols Polyols Acetals Oxacyclic compounds Organic oxides Aldehydes Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenolic glycoside - Benzophenone - Diphenylmethane - Aryl-phenylketone - O-glycosyl compound - Pentose monosaccharide - Phenoxy compound - Benzoyl - Phenol ether - Aryl ketone - Toluene - Oxane - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Secondary alcohol - Ketone - Polyol - Oxacycle - Acetal - Organoheterocyclic compound - Aldehyde - Hydrocarbon derivative - Organic oxide - Alcohol - Aromatic heteromonocyclic compound
Description
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.
External Descriptors
Not available