Compound Identification
SMILES
O[C@H]1[C@H](O)C2=C(O[C@@H]1C1=CC(O)=C(O)C(O)=C1)C=C(O)C(=C2)[C@@H]1[C@H](O)[C@H](OC2=C1C=CC(O)=C2)C1=CC(O)=C(O)C(O)=C1
InChIKey
InChIKey=GVBAISGMDHJZFT-QYWOBWDFSA-N
Formula
C30H26O13
Mass
594.525
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
-
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
B-type proanthocyanidins Leucoanthocyanidins Flavan-3-ols 7-hydroxyflavonoids 4-hydroxyflavonoids 4'-hydroxyflavonoids 3-hydroxyflavonoids 3'-hydroxyflavonoids 1-benzopyrans Pyrogallols and derivatives Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Secondary alcohols Polyols Oxacyclic compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
B-type proanthocyanidin - Proanthocyanidin - Bi- and polyflavonoid skeleton - Leucoanthocyanidin-skeleton - Hydroxyflavonoid - Flavan-3-ol - 7-hydroxyflavonoid - 4-hydroxyflavonoid - 4'-hydroxyflavonoid - 3-hydroxyflavonoid - 3'-hydroxyflavonoid - Flavan - 1-benzopyran - Benzopyran - Chromane - Pyrogallol derivative - Benzenetriol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - 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