Compound Identification
SMILES
CC1=C[C@H]([C@@H]([C@H](C1)C1=C(O)C=C(O)C=C1)C(=O)C1=C(O)C=C(O)C=C1)C1=C(O)C=CC(C2OC3=C(C=CC(O)=C3)C(=O)[C@@H]2O)=C1O
InChIKey
InChIKey=XFBBWTUEALDZHM-OVRHIZCTSA-N
Formula
C35H30O11
Mass
626.614
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Phenylpropanoids and polyketides
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Class
Flavonoids
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Subclass
Flavans
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Level 5
3'-prenylated flavans
- Level 6 3'-prenylated flavanones
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Level 5
3'-prenylated flavans
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Subclass
Flavans
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Class
Flavonoids
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Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Flavonoids
Subclass
Flavans
Intermediate Tree Nodes
3'-prenylated flavans
Direct Parent
3'-prenylated flavanones
Alternative Parents
Linear diarylheptanoids 3-hydroxyflavonoids 4'-hydroxyflavonoids 7-hydroxyflavonoids Flavanonols Alkyl-phenylketones Chromones Benzoyl derivatives Aryl alkyl ketones Resorcinols 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids Vinylogous acids Secondary alcohols Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
3'-prenylated flavanone - Linear 1,7-diphenylheptane skeleton - 3-hydroxyflavonoid - 4'-hydroxyflavonoid - 7-hydroxyflavonoid - Hydroxyflavonoid - Flavanonol - Flavanone - Alkyl-phenylketone - Chromone - Benzopyran - 1-benzopyran - Chromane - Phenylketone - Benzoyl - Aryl alkyl ketone - Aryl ketone - Resorcinol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Benzenoid - Monocyclic benzene moiety - Vinylogous acid - Secondary alcohol - Ketone - Ether - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alcohol - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 3'-prenylated flavanones. These are flavanones that features a C5-isoprenoid substituent at the 3'-position.
External Descriptors
Not available