Compound Identification
SMILES
CC(=O)C1=CC=C(CC2=CC=CC(=C2)[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1
InChIKey
InChIKey=QQOFNQUCIXOXLT-ADAARDCZSA-N
Formula
C21H24O6
Mass
372.417
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
Diphenylmethanes Alkyl-phenylketones Hexoses C-glycosyl compounds Acetophenones Benzoyl derivatives Aryl alkyl ketones Oxanes Secondary alcohols 1,2-diols Oxacyclic compounds Dialkyl ethers Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenolic glycoside - Alkyl-phenylketone - Diphenylmethane - Hexose monosaccharide - C-glycosyl compound - Acetophenone - Phenylketone - Benzoyl - Aryl ketone - Aryl alkyl ketone - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Oxane - Ketone - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Ether - Oxacycle - Dialkyl ether - Polyol - Alcohol - Hydrocarbon derivative - Organic oxide - Primary 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