Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](Oc2cc(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=RFZGXHLLXXDQJN-JNHRPPPUSA-N

Formula

C21H21Br3O10

Mass

673.101

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