Compound Identification
SMILES
COC1=CC2=C(OC(=O)C3=CC(C)=CC(OC)=C23)C2=C(C=CC(O)=C12)C1OC(C)C(O)C(C)(O)C1O
InChIKey
InChIKey=BJPYMDSMDBCKEP-UHFFFAOYSA-N
Formula
C27H28O9
Mass
496.512
Taxonomic Classification
Taxonomy Tree
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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
Naphthopyrans Coumarins and derivatives Naphthols and derivatives Isocoumarins and derivatives 1-benzopyrans 2-benzopyrans Anisoles 1-hydroxy-2-unsubstituted benzenoids Pyranones and derivatives Alkyl aryl ethers Oxanes Heteroaromatic compounds Tertiary alcohols Secondary alcohols Lactones Dialkyl ethers Oxacyclic compounds Polyols Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - Naphthopyran - 1-naphthol - Isocoumarin - Coumarin - Naphthalene - 1-benzopyran - 2-benzopyran - Benzopyran - Anisole - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Pyran - Oxane - Benzenoid - Tertiary alcohol - Heteroaromatic compound - Lactone - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Polyol - Organic oxide - 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