Compound Identification
SMILES
OC[C@H]1O[C@@](O)([C@H](OO)[C@@H](O)[C@@H]1O)C1=CC=CC2=C1C=CC1=CC=CC=C21
InChIKey
InChIKey=YECQFISGXQRKIA-OUUBHVDSSA-N
Formula
C20H20O7
Mass
372.373
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
Phenanthrenes and derivatives Naphthalenes Oxanes Monosaccharides Secondary alcohols Hemiacetals 1,2-diols Peroxols Oxacyclic compounds Alkyl hydroperoxides Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - Phenanthrene - Naphthalene - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Hydroperoxide - 1,2-diol - Hemiacetal - Polyol - Peroxol - Alkyl hydroperoxide - Organoheterocyclic compound - Oxacycle - Primary alcohol - Hydrocarbon derivative - Alcohol - Aromatic heteropolycyclic 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