Compound Identification
SMILES
CC1=CC2=C(OC1=O)C=C1C=C(C(=O)OC1=C2)C1=CC(=CC(=C1O)C(C)(C)C)C(C)(C)C
InChIKey
InChIKey=TZSFHGVZUPCOES-UHFFFAOYSA-N
Formula
C27H28O5
Mass
432.516
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
Isoflav-3-enones Hydroxyisoflavonoids Linear pyranocoumarins Pyranochromenes Phenylpropanes Pyranones and derivatives Phenols Heteroaromatic compounds Lactones Oxacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyranoisoflavonoid - Hydroxyisoflavonoid - Isoflav-3-enone skeleton - Pyranocoumarin - Linear pyranocoumarin - Pyranochromene - Coumarin - 1-benzopyran - Benzopyran - Phenylpropane - Phenol - Pyranone - Monocyclic benzene moiety - Pyran - Benzenoid - Heteroaromatic compound - Lactone - Oxacycle - Organoheterocyclic compound - 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