Structure Information
Structure

Compound Identification

SMILES

CC1(C)OC2=C(C=C1)C(O)=C(C(O)C1=CC=CC=C1)C1=C2C(=CC(=O)O1)C1=CC=CC=C1

InChIKey

InChIKey=QGFZHMDQSAXNLR-UHFFFAOYSA-N

Formula

C27H22O5

Mass

426.468

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Neoflavonoids

Subclass

Prenylated neoflavonoids

Intermediate Tree Nodes

Not available

Direct Parent

Prenylated neoflavonoids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Prenylated neoflavonoid - Linear 1,7-diphenylheptane skeleton - Pyranoneoflavonoid - 4-phenylcoumarin - Pyranocoumarin - Angular pyranocoumarin - 2,2-dimethyl-1-benzopyran - Coumarin - Benzopyran - 1-benzopyran - Pyranone - Alkyl aryl ether - Phenol - Monocyclic benzene moiety - Pyran - Benzenoid - Heteroaromatic compound - Lactone - Secondary alcohol - Organoheterocyclic compound - Ether - Oxacycle - Aromatic alcohol - Alcohol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

External Descriptors

Not available

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