Compound Identification
SMILES
CC1(C)OC2=C(C=C1)C(O)=C(C(O)C1=CC=CC=C1)C1=C2C(=CC(=O)O1)C1=CC=CC=C1
InChIKey
InChIKey=QGFZHMDQSAXNLR-UHFFFAOYSA-N
Formula
C27H22O5
Mass
426.468
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Neoflavonoids
- Subclass Prenylated neoflavonoids
-
Class
Neoflavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Neoflavonoids
Subclass
Prenylated neoflavonoids
Intermediate Tree Nodes
Not available
Direct Parent
Prenylated neoflavonoids
Alternative Parents
Linear diarylheptanoids Pyranoneoflavonoids Neoflavones Angular pyranocoumarins 2,2-dimethyl-1-benzopyrans Alkyl aryl ethers Pyranones and derivatives Phenols Benzene and substituted derivatives Heteroaromatic compounds Lactones Secondary alcohols Oxacyclic compounds Hydrocarbon derivatives Aromatic alcohols Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Prenylated neoflavonoid - Linear 1,7-diphenylheptane skeleton - Pyranoneoflavonoid - 4-phenylcoumarin - Pyranocoumarin - Angular pyranocoumarin - 2,2-dimethyl-1-benzopyran - Coumarin - Benzopyran - 1-benzopyran - Pyranone - Alkyl aryl ether - Phenol - Monocyclic benzene moiety - Pyran - Benzenoid - Heteroaromatic compound - Lactone - Secondary alcohol - Organoheterocyclic compound - Ether - Oxacycle - Aromatic alcohol - Alcohol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
External Descriptors
Not available