Compound Identification
SMILES
OC[C@H]1O[C@@H](OC2=CC3=C(C=C2)C(=CC(=O)O3)C2=CC=CC=C2)[C@H](O)[C@@H](O)[C@H]1O
InChIKey
InChIKey=SGRGSGBBTICBSH-OBJCFNGXSA-N
Formula
C21H20O8
Mass
400.383
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Neoflavonoids
- Subclass Neoflavonoid 7-O-glycosides
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Class
Neoflavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Neoflavonoids
Subclass
Neoflavonoid 7-O-glycosides
Intermediate Tree Nodes
Not available
Direct Parent
Neoflavonoid 7-O-glycosides
Alternative Parents
Coumarin glycosides Neoflavones Phenolic glycosides Hexoses O-glycosyl compounds 1-benzopyrans Pyranones and derivatives Oxanes Benzene and substituted derivatives Heteroaromatic compounds Lactones Secondary alcohols Oxacyclic compounds Acetals Polyols Organic oxides Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Neoflavonoid-7-o-glycoside - Coumarin-7-o-glycoside - Coumarin o-glycoside - 4-phenylcoumarin - Phenolic glycoside - Hexose monosaccharide - Coumarin - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Pyranone - Oxane - Pyran - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Heteroaromatic compound - Secondary alcohol - Lactone - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - Primary alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as neoflavonoid 7-o-glycosides. These are 7-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
External Descriptors
Not available