Compound Identification
SMILES
COC1=CC=C(C=C1)C1=C(C)C2=C(OC1=O)C1=C(OC(=O)C(=C1C)C1=CC=C(OC)C=C1)C=C2
InChIKey
InChIKey=VPTASEFJLIMCRV-UHFFFAOYSA-N
Formula
C28H22O6
Mass
454.478
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 Phenoxy compounds Methoxybenzenes Anisoles Pyranones and derivatives Alkyl aryl ethers Heteroaromatic compounds Lactones Oxacyclic 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 - 1-benzopyran - Benzopyran - Anisole - Phenol ether - Phenoxy compound - Methoxybenzene - Pyranone - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Pyran - Heteroaromatic compound - 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 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