Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)OCCOC1=C(O[C@@H]2CCCCO2)C=CC2=C1OC(=O)C=C2C1=CC=CC=C1

InChIKey

InChIKey=SWKZFKCENBPNNT-HHHXNRCGSA-N

Formula

C29H28O8S

Mass

536.6

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Neoflavonoids

Subclass

Neoflavonoid 7-O-glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Neoflavonoid 7-O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Neoflavonoid-7-o-glycoside - Coumarin o-glycoside - Coumarin-7-o-glycoside - 4-phenylcoumarin - Benzenesulfonate ester - Coumarin - P-methylbenzenesulfonate - Benzenesulfonate - Tosyl compound - 1-benzopyran - Benzopyran - Benzenesulfonyl group - Arylsulfonic acid or derivatives - Pyranone - Toluene - Alkyl aryl ether - Oxane - Organosulfonic acid ester - Monocyclic benzene moiety - Pyran - Benzenoid - Heteroaromatic compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Lactone - Ether - Organoheterocyclic compound - Oxacycle - Acetal - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organosulfur compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as neoflavonoid 7-o-glycosides. These are 7-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

External Descriptors

Not available

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