Compound Identification
SMILES
CC(C1=C(O)C2=CC=CC=C2C=C1)=C1C(=O)OC2=C(C=CC3=CC=CC=C23)C1=O
InChIKey
InChIKey=HBSBVHIOMQGELO-UHFFFAOYSA-N
Formula
C25H16O4
Mass
380.399
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Homoisoflavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Homoisoflavonoids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Homoisoflavonoids
Alternative Parents
Naphthopyranones Benzochromones Naphthols and derivatives 3,4-dihydrocoumarins Aryl ketones 1-hydroxy-4-unsubstituted benzenoids Pyrans Enoate esters Lactones Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Aldehydes
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homoisoflavonoid - Benzochromone - Naphthopyranone - Naphthopyran - 3,4-dihydrocoumarin - Chromone - 1-naphthol - Chromane - Benzopyran - Naphthalene - 1-benzopyran - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - Benzenoid - Pyran - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Lactone - Ketone - Carboxylic acid ester - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aldehyde - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as homoisoflavonoids. These are naturally occurring oxygen heterocycles with a structure based on a 16-carbon skeleton including a chromanone, chromone or chromane system with a benzyl group at position C-3.
External Descriptors
Not available