Compound Identification
SMILES
OCC1=CC=CC=C1O[C@@H]1O[C@@H]2CO[C@H](O[C@H]2[C@H](O)[C@H]1O)C1=CC=CC=C1
InChIKey
InChIKey=BLJNLDHHNYZHTB-BZIXAJQCSA-N
Formula
C20H22O7
Mass
374.389
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
Pyranodioxins Phenoxy compounds Phenol ethers Benzyl alcohols Oxanes Monosaccharides 1,3-dioxanes Secondary alcohols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives Aromatic alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - Pyranodioxin - Phenoxy compound - Benzyl alcohol - Phenol ether - Meta-dioxane - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Acetal - Alcohol - Hydrocarbon derivative - Primary alcohol - Aromatic 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