Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1C2CC3C(C)(C)O[C@](C\C=C(\C)C(O)=O)(C2=O)C32OC3=C(C(=O)[C@@H]12)C(O)=C1C=CC(C)(C)OC1=C3CC(O)C(C)(C)O

InChIKey

InChIKey=YACUINUOCLLMGT-ZIHZHPONSA-N

Formula

C34H42O11

Mass

626.699

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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 alkyl ketones Alkyl aryl ethers Oxepanes Benzenoids Vinylogous acids Tertiary alcohols Oxolanes Secondary alcohols 1,2-diols Carboxylic acids Oxacyclic compounds Dialkyl ethers Monocarboxylic acids and derivatives Organic oxides Aldehydes Hydrocarbon derivatives

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyranoxanthone - Pyranochromene - 2,2-dimethyl-1-benzopyran - Chromone - Monoterpenoid - Aromatic monoterpenoid - Aryl alkyl ketone - Aryl ketone - Alkyl aryl ether - Oxepane - Benzenoid - Vinylogous acid - Oxolane - Tertiary alcohol - Ketone - Secondary alcohol - 1,2-diol - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Organic oxygen compound - Carbonyl group - Alcohol - Aldehyde - Organic oxide - Organooxygen compound - Hydrocarbon derivative - 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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