Compound Identification
SMILES
COC1=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C2C(=O)C(C(C)=O)=C(C)C(=O)C2=C1
InChIKey
InChIKey=GVMOOQOCLYWVKF-BNCZOOBYSA-N
Formula
C20H22O10
Mass
422.386
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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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
Hexoses Naphthoquinones O-glycosyl compounds Anisoles Aryl ketones Quinones Alkyl aryl ethers Oxanes Secondary alcohols Acetals Oxacyclic compounds Polyols Organic oxides Primary alcohols Hydrocarbon derivatives Aldehydes
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - Hexose monosaccharide - Naphthoquinone - O-glycosyl compound - Naphthalene - Anisole - Aryl ketone - Quinone - Alkyl aryl ether - Monosaccharide - Benzenoid - Oxane - Secondary alcohol - Ketone - Organoheterocyclic compound - Acetal - Oxacycle - Ether - Polyol - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aldehyde - Primary 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