Structure Information
Structure

Compound Identification

SMILES

[H][C@@]1(CC2=C(O1)C=CC1=C2O[C@]2([H])COC3=CC(OC)=C(OC)C=C3[C@@]2([H])C1=O)[C@@](C)(O)CO[C@]1([H])O[C@]([H])(CO)[C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O

InChIKey

InChIKey=FTHIJITZGQUCNU-TYSHFJKBSA-N

Formula

C29H34O13

Mass

590.578

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Flavonoid O-glycosides

Direct Parent

Rotenoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Rotenoid-8p-o-glycoside - Rotenone or derivatives - 8-prenylated isoflavanone - Chromeno-3,4b-chromene - Rotenoid - Isoflavanone - Isoflavan - Isoflavonoid - Hexose monosaccharide - Chromone - Glycosyl compound - O-glycosyl compound - 1-benzopyran - Chromane - Benzopyran - Coumaran - Aryl alkyl ketone - Aryl ketone - Anisole - Alkyl aryl ether - Benzenoid - Oxane - Monosaccharide - Tertiary alcohol - Secondary alcohol - Ketone - Organoheterocyclic compound - Oxacycle - Polyol - Acetal - Ether - Hydrocarbon derivative - Organooxygen compound - Primary alcohol - Alcohol - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as rotenoid o-glycosides. These are compounds containing a carbohydrate moiety glycosidically linked to the rotenoid backbone at the C8-position.

External Descriptors

Not available

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