Compound Identification
SMILES
O=C1OC2=C(C3=C(C=C2)C(\C=C\C2=CC=CC=C2)=C(C(=O)O3)C2=CC=CC=C2)C(\C=C\C2=CC=CC=C2)=C1C1=CC=CC=C1
InChIKey
InChIKey=AHXCDYVDPYJXET-MBALSZOMSA-N
Formula
C40H26O4
Mass
570.644
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Phenylpropanoids and polyketides
-
Class
Isoflavonoids
- Subclass Pyranoisoflavonoids
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Class
Isoflavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Isoflavonoids
Subclass
Pyranoisoflavonoids
Intermediate Tree Nodes
Not available
Direct Parent
Pyranoisoflavonoids
Alternative Parents
Linear diarylheptanoids Isoflav-3-enones Angular pyranocoumarins 1-benzopyrans Styrenes Pyranones and derivatives Heteroaromatic compounds Lactones Oxacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyranoisoflavonoid - Linear 1,7-diphenylheptane skeleton - Isoflav-3-enone skeleton - Angular pyranocoumarin - Pyranocoumarin - Coumarin - Benzopyran - 1-benzopyran - Styrene - Pyranone - Monocyclic benzene moiety - Benzenoid - Pyran - Heteroaromatic compound - Lactone - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton.
External Descriptors
Not available