You are using an unsupported browser. Please upgrade your browser to a newer version to get the best experience on ClassyFire.
Structure Information
Structure

Compound Identification

SMILES

COC1=C(O)C=CC(=C1)[C@@H]1OC2=C(O[C@H]1CO)C=CC(=C2)[C@@H]1OC2=CC(O)=CC(O)=C2C(=O)[C@H]1C

InChIKey

InChIKey=QAAGQVSKJNEYRJ-AQJFPPKMSA-N

Formula

C26H24O9

Mass

480.469

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lignans, neolignans and related compounds

Class

Flavonolignans

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Flavonolignans

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonolignan - Hydroxyflavonoid - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Flavanone - Flavan - 2-phenylbenzo-1,4-dioxane - Phenylbenzodioxane - Chromone - Methoxyphenol - Benzo-1,4-dioxane - Benzodioxane - Chromane - 1-benzopyran - Benzopyran - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Aryl ketone - Aryl alkyl ketone - Alkyl aryl ether - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Benzenoid - Para-dioxin - Vinylogous acid - Ketone - Organoheterocyclic compound - Oxacycle - Ether - Alcohol - Primary alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - 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

Previous Back Next