Compound Identification
SMILES
[H][C@@]1(CC2=C(O1)C=CC1=C2OC2=C(C1=O)C1=CC(OC)=C(OC)C=C1OC2)C(C)(C)O[C@@]1([H])O[C@@]([H])(CO)[C@]([H])(O)[C@@]([H])(O)[C@]1([H])O
InChIKey
InChIKey=FLVHSTRJNNFIPP-XEVNROCBSA-N
Formula
C29H32O12
Mass
572.563
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Isoflavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Isoflavonoids
Subclass
Rotenoids
Intermediate Tree Nodes
Not available
Direct Parent
Rotenones
Alternative Parents
Isoflavones Hexoses Chromones O-glycosyl compounds Coumarans Anisoles Pyranones and derivatives Alkyl aryl ethers Oxanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Polyols Acetals Organic oxides Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Rotenone or derivatives - Isoflavone - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Chromone - Benzopyran - 1-benzopyran - Coumaran - Anisole - Alkyl aryl ether - Pyranone - Monosaccharide - Pyran - Oxane - Benzenoid - Heteroaromatic compound - Secondary alcohol - Acetal - Oxacycle - Ether - Organoheterocyclic compound - Polyol - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Primary alcohol - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as rotenones. These are rotenoids with a structure based on a 6a,12a-dihydrochromeno[3,4-b]chromen-12(6H)-one skeleton.
External Descriptors
Not available