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Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCC(=O)OC1=CC(O)=C2C(=O)[C@H](O)[C@H](OC2=C1)C1=CC2=C(OC(CO)C(O2)C2=CC(OC)=C(O)C=C2)C=C1

InChIKey

InChIKey=WPMFGQMFMQCEOY-AGJTWYCZSA-N

Formula

C41H52O11

Mass

720.856

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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 - Flavanonol - 3-hydroxyflavonoid - 5-hydroxyflavonoid - Flavanone - Phenylbenzodioxane - 2-phenylbenzo-1,4-dioxane - Flavan - Chromone - Benzopyran - Phenol ester - Methoxyphenol - Benzo-1,4-dioxane - Chromane - 1-benzopyran - Benzodioxane - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Aryl alkyl ketone - Aryl ketone - Fatty acid ester - Alkyl aryl ether - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Fatty acyl - Monocyclic benzene moiety - Benzenoid - Para-dioxin - Vinylogous acid - Carboxylic acid ester - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Primary alcohol - Organic oxide - Organooxygen compound - Alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxygen 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

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