Compound Identification
SMILES
COC1=CC2=C(C=C1)[C@@]1(O)[C@@H](CO2)OC2=C(C=CC(O)=C2)C1C1=C(OC)C=CC(=C1)[C@@H]1COC2=C(C1)C=CC(O)=C2
InChIKey
InChIKey=AAYNXSSLTTZFMB-PUVHLHJNSA-N
Formula
C33H30O8
Mass
554.595
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Isoflavonoids
- Subclass Rotenoids
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Class
Isoflavonoids
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Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Isoflavonoids
Subclass
Rotenoids
Intermediate Tree Nodes
Not available
Direct Parent
Rotenoids
Alternative Parents
4'-O-methylated isoflavonoids Lignans, neolignans and related compounds Isoflavanols Hydroxyisoflavonoids Neoflavans 1-benzopyrans Phenoxy compounds Methoxybenzenes Anisoles Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Tertiary alcohols Oxacyclic compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Chromeno-3,4b-chromene - 4p-methoxyisoflavonoid - Rotenoid - Hydroxyisoflavonoid - Isoflavanol - Neolignan skeleton - Isoflavan - Neoflavan - Chromane - Benzopyran - 1-benzopyran - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Benzenoid - Tertiary alcohol - Organoheterocyclic compound - Oxacycle - Ether - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as rotenoids. These are phenolic compounds containing a cis-fused tetrahydrochromeno[3,4-b]chromene nucleus. Many rotenoids contain an additional ring, e.g. rotenone. They are isoflavonoids characterized by the presence of an extra carbon atom in an additional heterocyclic ring.
External Descriptors
Not available