Compound Identification
SMILES
COC1=CC=C(\C=C\C2=C(C(=O)OC3=CC4=C(C=C23)C(C)=C(O4)C(=O)C2=CC=CC=C2)C2=CC=CC=C2)C=C1
InChIKey
InChIKey=SERKKQQEZMGEOT-OBGWFSINSA-N
Formula
C34H24O5
Mass
512.561
Taxonomic Classification
Taxonomy Tree
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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
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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 Phenoxy compounds Methoxybenzenes Anisoles Benzoyl derivatives Pyranones and derivatives Alkyl aryl ethers Heteroaromatic compounds Furans Lactones Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Furanoisoflavonoid skeleton - Isoflav-3-enone skeleton - Furanocoumarin - Linear furanocoumarin - Psoralen - Aryl-phenylketone - Coumarin - Benzopyran - 1-benzopyran - Benzofuran - Phenoxy compound - Anisole - Benzoyl - Phenol ether - Methoxybenzene - Styrene - Aryl ketone - Alkyl aryl ether - Pyranone - Monocyclic benzene moiety - Pyran - Benzenoid - Heteroaromatic compound - Furan - Ketone - Lactone - Oxacycle - Organoheterocyclic compound - Ether - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen 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