Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](Oc2c(Br)c(O)c(Br)c(O)c2C(=O)CCc2cc(Br)c(O)c(Br)c2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=FINNPFQSLRPSQZ-CFNLRIOXSA-N

Formula

C21H20Br4O10

Mass

751.997

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Flavonoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Flavonoid o-glycoside - 2'-hydroxy-dihydrochalcone - Phenolic glycoside - Linear 1,3-diarylpropanoid - Cinnamylphenol - Alkyl-phenylketone - Hexose monosaccharide - Butyrophenone - Glycosyl compound - O-glycosyl compound - Phenylketone - Benzoyl - Phenoxy compound - 4-halophenol - 2-halophenol - 2-bromophenol - 4-bromophenol - Phenol ether - Resorcinol - Aryl alkyl ketone - Aryl ketone - Bromobenzene - Phenol - Halobenzene - Benzenoid - Monocyclic benzene moiety - Oxane - Aryl halide - Monosaccharide - Aryl bromide - Vinylogous acid - Secondary alcohol - Ketone - Acetal - Organoheterocyclic compound - Polyol - Oxacycle - Alcohol - Primary alcohol - Organohalogen compound - Organobromide - Organic oxygen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid o-glycosides. These are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.

External Descriptors

Not available

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