Compound Identification
SMILES
COC(=O)CC1=CC=CC2=C1OC(C(C(=O)C1=CC=CC=C1)C2=O)C1=CC=CC=C1
InChIKey
InChIKey=HHDDVOQELDDLFL-UHFFFAOYSA-N
Formula
C25H20O5
Mass
400.43
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Phenylpropanoids and polyketides
-
Class
Homoisoflavonoids
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Subclass
Homoisoflavans
- Level 5 Homoisoflavanones
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Subclass
Homoisoflavans
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Class
Homoisoflavonoids
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Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Homoisoflavonoids
Subclass
Homoisoflavans
Intermediate Tree Nodes
Not available
Direct Parent
Homoisoflavanones
Alternative Parents
Flavanones Alkyl-phenylketones Chromones Benzoyl derivatives Aryl alkyl ketones Beta-diketones Alkyl aryl ethers Methyl esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homoisoflavanone - Flavanone - Flavan - Alkyl-phenylketone - Chromone - Chromane - Benzopyran - 1-benzopyran - Phenylketone - Benzoyl - Aryl alkyl ketone - Aryl ketone - Alkyl aryl ether - 1,3-diketone - Monocyclic benzene moiety - 1,3-dicarbonyl compound - Benzenoid - Methyl ester - Carboxylic acid ester - Ketone - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Ether - Carbonyl group - Organic oxide - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as homoisoflavanones. These are homoisoflavonoids with a structure based on the chromanone system. Chromanone is a bicyclic compound consisting of a 3,4-dihydro-1-benzopyran, which bears a ketone group at the 4-position.
External Descriptors
Not available