Compound Identification
SMILES
C[C@H]1OC2=C(C(=O)[C@H]1C)C1=C(C(O)=C2CC=C)C(=CC(=O)O1)C1=CC=CC=C1
InChIKey
InChIKey=CXUHIQGZWKAHRL-QWHCGFSZSA-N
Formula
C23H20O5
Mass
376.408
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Neoflavonoids
- Subclass Pyranoneoflavonoids
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Class
Neoflavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Neoflavonoids
Subclass
Pyranoneoflavonoids
Intermediate Tree Nodes
Not available
Direct Parent
Pyranoneoflavonoids
Alternative Parents
Neoflavones Angular pyranocoumarins Pyranochromenes Chromones Aryl alkyl ketones Pyranones and derivatives Phenols Alkyl aryl ethers Benzene and substituted derivatives Heteroaromatic compounds Lactones Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyranoneoflavonoid - 4-phenylcoumarin - Angular pyranocoumarin - Pyranocoumarin - Pyranochromene - Chromone - Coumarin - Chromane - Benzopyran - 1-benzopyran - Aryl alkyl ketone - Aryl ketone - Alkyl aryl ether - Phenol - Pyranone - Monocyclic benzene moiety - Benzenoid - Pyran - Heteroaromatic compound - Lactone - Ketone - Organoheterocyclic compound - Ether - Oxacycle - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pyranoneoflavonoids. These are compounds containing a pyran ring fused to either ring A, B, or C of the neoflavonoid skeleton. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
External Descriptors
Not available