Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1OC(OC2=CC3=C(C=C2)C(=O)C(=CO3)C2=CC=C(OS(O)(=O)=O)C=C2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O

InChIKey

InChIKey=YLYDFNVTVUNKCE-UHFFFAOYSA-N

Formula

C28H26O16S

Mass

650.56

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Isoflavonoids

Subclass

Isoflavonoid O-glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Isoflavonoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Isoflavonoid-7-o-glycoside - Isoflavonoid o-glycoside - Isoflavone - Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Tetracarboxylic acid or derivatives - Glucuronic acid or derivatives - Phenylsulfate - O-glycosyl compound - Glycosyl compound - Chromone - Arylsulfate - 1-benzopyran - Benzopyran - Phenoxy compound - Pyranone - Benzenoid - Sulfuric acid ester - Sulfate-ester - Sulfuric acid monoester - Pyran - Oxane - Monosaccharide - Monocyclic benzene moiety - Heteroaromatic compound - Methyl ester - Organic sulfuric acid or derivatives - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.

External Descriptors

Not available

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