Compound Identification
SMILES
COC(=O)C1=CC(\C=C2\C(=O)C3=C(OC2(C)C)C=CC(OCC2=CC=CC=C2)=C3)=C(OC)C=C1
InChIKey
InChIKey=ZVELDYZCECYIPP-HAHDFKILSA-N
Formula
C28H26O6
Mass
458.51
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
2,2-dimethyl-1-benzopyrans P-methoxybenzoic acids and derivatives Chromones Benzoic acid esters Phenoxy compounds Methoxybenzenes Benzoyl derivatives Aryl ketones Anisoles Alkyl aryl ethers Methyl esters Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Homoisoflavonoid - 2,2-dimethyl-1-benzopyran - Chromone - P-methoxybenzoic acid or derivatives - Benzoate ester - Chromane - Benzopyran - 1-benzopyran - Benzoic acid or derivatives - Anisole - Phenoxy compound - Benzoyl - Methoxybenzene - Phenol ether - Aryl ketone - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Methyl ester - Ketone - Carboxylic acid ester - Ether - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen 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