Compound Identification
SMILES
CC1=C(C(=O)OC2=C1C=CC1=C2C(C)=C(C(=O)O1)C1=CC=C(Cl)C=C1)C1=CC=C(Cl)C=C1
InChIKey
InChIKey=JOQZNGXLJHLISE-UHFFFAOYSA-N
Formula
C26H16Cl2O4
Mass
463.31
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Isoflavonoids
- Subclass Pyranoisoflavonoids
-
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 Chlorobenzenes Aryl chlorides Heteroaromatic compounds Lactones Oxacyclic compounds Organooxygen compounds Organochlorides 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 - Chlorobenzene - Halobenzene - Pyranone - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyran - Heteroaromatic compound - Lactone - Oxacycle - Organoheterocyclic compound - Organic oxide - Organic oxygen compound - Organohalogen compound - Organochloride - Organooxygen compound - Hydrocarbon derivative - 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