Compound Identification
SMILES
COC1=CC=C(C=C1)[C@H]1OC2=C3C4[C@@H](O)[C@@](OC5=CC(OC)=CC(OC)=C45)(OC3=CC(OC)=C2C[C@@H]1O)C1=CC(OC)=C(OC)C=C1
InChIKey
InChIKey=LKTHMIWWFDQHGR-ASVJSXPTSA-N
Formula
C36H36O11
Mass
644.673
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
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Class
Flavonoids
- Subclass Biflavonoids and polyflavonoids
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Class
Flavonoids
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Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Flavonoids
Subclass
Biflavonoids and polyflavonoids
Intermediate Tree Nodes
Not available
Direct Parent
Biflavonoids and polyflavonoids
Alternative Parents
A-type proanthocyanidins Catechins Pyranoflavonoids 3'-O-methylated flavonoids 4'-O-methylated flavonoids 5-O-methylated flavonoids 7-O-methylated flavonoids 3-hydroxyflavonoids Pyranochromenes Dimethoxybenzenes Anisoles Phenoxy compounds Alkyl aryl ethers Ketals Secondary alcohols Oxacyclic compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
A-type proanthocyanidin - Bi- and polyflavonoid skeleton - Proanthocyanidin - Catechin - Pyranoflavonoid - 3p-methoxyflavonoid-skeleton - 4p-methoxyflavonoid-skeleton - 5-methoxyflavonoid-skeleton - 7-methoxyflavonoid-skeleton - 3-hydroxyflavonoid - Flavan-3-ol - Hydroxyflavonoid - Flavan - Pyranochromene - Chromane - Benzopyran - O-dimethoxybenzene - Dimethoxybenzene - 1-benzopyran - Anisole - Methoxybenzene - Phenol ether - Phenoxy compound - Alkyl aryl ether - Ketal - Monocyclic benzene moiety - Benzenoid - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Acetal - Ether - Organooxygen compound - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''.
External Descriptors
Not available