Compound Identification
SMILES
OC1=CC=C(\C=C\C2=C(C(=O)OC3=C2C=CC2=C3C(\C=C\C3=CC=C(O)C=C3)=C(C(=O)O2)C2=CC=CC=C2)C2=CC=CC=C2)C=C1
InChIKey
InChIKey=GUJKQTSXBNJAQV-YHARCJFQSA-N
Formula
C40H26O6
Mass
602.642
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
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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 1-hydroxy-2-unsubstituted benzenoids 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 - Pyranocoumarin - Angular pyranocoumarin - Coumarin - Benzopyran - 1-benzopyran - Styrene - Pyranone - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Pyran - Benzenoid - Heteroaromatic compound - Lactone - Oxacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen 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