Structure Information
Structure

Compound Identification

SMILES

CC(C)=CCc1c2O[C@@]34[C@H]5C[C@@H](C=C3C(=O)c2c(O)c2C=CC(C)(C)Oc12)C(=O)[C@]4(C\C=C(\C)C([O-])=O)OC5(C)C

InChIKey

InChIKey=COVMVPHACFXMAX-OYNOKLRGSA-M

Formula

C33H35O8

Mass

559.636

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Benzopyrans

Subclass

1-benzopyrans

Intermediate Tree Nodes

Dibenzopyrans - Xanthenes - Xanthones

Direct Parent

Pyranoxanthones

Alternative Parents

Pyranochromenes 2,2-dimethyl-1-benzopyrans Chromones Aromatic monoterpenoids Aryl ketones Oxepanes Alkyl aryl ethers Cyclohexenones Benzenoids Vinylogous acids Tetrahydrofurans Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Dialkyl ethers Hydrocarbon derivatives Organic oxides Organic anions

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyranoxanthone - Pyranochromene - 2,2-dimethyl-1-benzopyran - Chromone - Aromatic monoterpenoid - Monoterpenoid - Aryl ketone - Alkyl aryl ether - Cyclohexenone - Oxepane - Benzenoid - Vinylogous acid - Tetrahydrofuran - Ketone - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Organic oxide - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organic anion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system.

External Descriptors

Not available

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