Compound Identification
SMILES
CC(C)=CCC\C(C)=C\CC1=C(C=CC(O)=C1O)[C@@H]1CC(=O)C2=C(O1)C=C1OC(C)(C)C=CC1=C2O
InChIKey
InChIKey=NWOAUZRIIYJJIS-AVQBUJNVSA-N
Formula
C30H34O6
Mass
490.596
Taxonomic Classification
Taxonomy Tree
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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
2'-prenylated flavans
- Level 6 2'-prenylated flavanones
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Level 5
2'-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
2'-prenylated flavans
Direct Parent
2'-prenylated flavanones
Alternative Parents
Pyranoflavonoids 3'-hydroxyflavonoids Flavanones 4'-hydroxyflavonoids 5-hydroxyflavonoids Pyranochromenes 2,2-dimethyl-1-benzopyrans Chromones Aromatic monoterpenoids Catechols Aryl alkyl ketones 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Alkyl aryl ethers Benzene and substituted derivatives Vinylogous acids Oxacyclic compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
2'-prenylated flavanone - Pyranoflavonoid - 3'-hydroxyflavonoid - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - Flavanone - Hydroxyflavonoid - Pyranochromene - 2,2-dimethyl-1-benzopyran - Chromone - Aromatic monoterpenoid - Chromane - Benzopyran - Monoterpenoid - 1-benzopyran - Catechol - Aryl alkyl ketone - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Monocyclic benzene moiety - Benzenoid - Vinylogous acid - Ketone - Ether - Organoheterocyclic compound - Oxacycle - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 2'-prenylated flavanones. These are flavanones that features a C5-isoprenoid substituent at the 2'-position.
External Descriptors
Not available