Compound Identification
SMILES
CC1=C(OC2=C1C=C1C(OC(=O)C(C3=CC=CC=C3)=C1\C=C\C1=CC=C(Cl)C=C1)=C2)C(=O)C1=CC=CC=C1
InChIKey
InChIKey=PFGYNIDBMJNGOS-SAPNQHFASA-N
Formula
C33H21ClO4
Mass
516.98
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
Furanoisoflavonoids Psoralens Aryl-phenylketones 1-benzopyrans Benzofurans Styrenes Benzoyl derivatives Pyranones and derivatives Chlorobenzenes Aryl chlorides Heteroaromatic compounds Furans Lactones Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organochlorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Furanoisoflavonoid skeleton - Isoflav-3-enone skeleton - Furanocoumarin - Psoralen - Linear furanocoumarin - Aryl-phenylketone - Coumarin - Benzopyran - 1-benzopyran - Benzofuran - Benzoyl - Aryl ketone - Styrene - Chlorobenzene - Halobenzene - Pyranone - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyran - Furan - Heteroaromatic compound - Ketone - Lactone - Organoheterocyclic compound - Oxacycle - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organochloride - Organohalogen 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