Compound Identification
SMILES
O=C1OC2=C(C3=C(C=C2)C(\C=C\C2=CC=CO2)=C(C(=O)O3)C2=CC=CC=C2)C(\C=C\C2=CC=CO2)=C1C1=CC=CC=C1
InChIKey
InChIKey=KWOXGALOWQWKIF-YTEMWHBBSA-N
Formula
C36H22O6
Mass
550.566
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
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 Pyranones and derivatives Benzene and substituted derivatives Heteroaromatic compounds Furans 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 - Pyranone - Monocyclic benzene moiety - Pyran - Benzenoid - Heteroaromatic compound - Furan - Lactone - Oxacycle - Organoheterocyclic compound - Organooxygen compound - Hydrocarbon derivative - 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