Compound Identification
SMILES
O=C(NC1=CC2=C(C=C1)C(=O)C1=CC=CC=C1C2=O)C1=CC=C(C=C1)C1=CC2=CC=CC=C2OC1=O
InChIKey
InChIKey=ZJTAWOSBMSDHSG-UHFFFAOYSA-N
Formula
C30H17NO5
Mass
471.468
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Phenylpropanoids and polyketides
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Class
Isoflavonoids
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Subclass
Isoflav-3-enes
- Level 5 Isoflav-3-enones
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Subclass
Isoflav-3-enes
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Class
Isoflavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Isoflavonoids
Subclass
Isoflav-3-enes
Intermediate Tree Nodes
Not available
Direct Parent
Isoflav-3-enones
Alternative Parents
Anthraquinones Coumarins and derivatives 1-benzopyrans Benzamides Aryl ketones Benzoyl derivatives Pyranones and derivatives Heteroaromatic compounds Secondary carboxylic acid amides Lactones Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Aldehydes Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Isoflav-3-enone skeleton - 9,10-anthraquinone - Anthraquinone - Anthracene - Coumarin - Benzopyran - 1-benzopyran - Benzamide - Benzoic acid or derivatives - Aryl ketone - Benzoyl - Pyranone - Monocyclic benzene moiety - Benzenoid - Pyran - Heteroaromatic compound - Carboxamide group - Lactone - Secondary carboxylic acid amide - Ketone - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Aldehyde - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as isoflav-3-enones. These are flavonoids with a structure based on an isoflav-3-ene skeleton bearing an oxo-group at position C2.
External Descriptors
Not available