Compound Identification
SMILES
COC1=CC(=CC2=C1OC(C(CO)O2)C1=CC(OC)=C(O)C=C1)C1=CC(=O)C2=CC=CC=C2O1
InChIKey
InChIKey=WQXOJVFNBZCZOL-UHFFFAOYSA-N
Formula
C26H22O8
Mass
462.454
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lignans, neolignans and related compounds
- Class Flavonolignans
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Superclass
Lignans, neolignans and related compounds
Kingdom
Organic compounds
Superclass
Lignans, neolignans and related compounds
Class
Flavonolignans
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Flavonolignans
Alternative Parents
3'-O-methylated flavonoids Flavones Phenylbenzo-1,4-dioxanes Chromones Benzo-1,4-dioxanes Methoxyphenols Anisoles Phenoxy compounds Methoxybenzenes Pyranones and derivatives 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Para dioxins Heteroaromatic compounds Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Flavonolignan - 3p-methoxyflavonoid-skeleton - Flavone - 2-phenylbenzo-1,4-dioxane - Phenylbenzodioxane - Chromone - Benzo-1,4-dioxane - Benzodioxane - Benzopyran - 1-benzopyran - Methoxyphenol - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Pyranone - Phenol - Pyran - Benzenoid - Monocyclic benzene moiety - Para-dioxin - Heteroaromatic compound - Organoheterocyclic compound - Ether - Oxacycle - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic oxygen compound - Primary alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as flavonolignans. These are non-conventional lignans that derived from flavonoids. They are characterized by a p-dioxin ring substituted at one carbon atom by a C3C6 (phenylpropan) group and fused to the B-ring of the 2-phenylchromene moiety.
External Descriptors
Not available