Compound Identification
SMILES
COC1C(OC)C2=C(OC1C1=CC=C(O)C=C1)C=C1OC(C)(C)C=CC1=C2OC
InChIKey
InChIKey=KAMSUIMVPLJLGA-UHFFFAOYSA-N
Formula
C23H26O6
Mass
398.455
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Flavonoids
- Subclass Pyranoflavonoids
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Class
Flavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Flavonoids
Subclass
Pyranoflavonoids
Intermediate Tree Nodes
Not available
Direct Parent
Pyranoflavonoids
Alternative Parents
Leucoanthocyanidins 5-O-methylated flavonoids 4-O-methylated flavonoids 3-O-methylated flavonoids Monohydroxyflavonoids 4'-hydroxyflavonoids Pyranochromenes 2,2-dimethyl-1-benzopyrans Anisoles Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Oxacyclic compounds Dialkyl ethers Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyranoflavonoid - 3-methoxyflavonoid-skeleton - 4-methoxyflavonoid-skeleton - 5-methoxyflavonoid-skeleton - Leucoanthocyanidin-skeleton - 4'-hydroxyflavonoid - Hydroxyflavonoid - Monohydroxyflavonoid - Flavan - Pyranochromene - 2,2-dimethyl-1-benzopyran - 1-benzopyran - Chromane - Benzopyran - Phenol ether - Anisole - Phenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Monocyclic benzene moiety - Oxacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pyranoflavonoids. These are compounds containing a pyran ring fused to a 2-phenyl-1,4-benzopyran skeleton.
External Descriptors
Not available