Structure Information
Structure

Compound Identification

SMILES

C[C@H]1O[C@@H](CC[C@H]1O)O[C@@]12C(=O)[C@@H](O)[C@](C)(O)C[C@]1(O)C=CC1=C2C(=O)c2cccc(O)c2C1=O

InChIKey

InChIKey=CKZNKYSWWCSICZ-FYJHTGLRSA-N

Formula

C25H26O10

Mass

486.473

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Benzenoids

Class

Anthracenes

Subclass

Anthraquinones

Intermediate Tree Nodes

Not available

Direct Parent

Anthraquinone glycosides

Alternative Parents

Angucyclines Hydroxyanthraquinones Naphthalenes Quinones Aryl ketones 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Oxanes Vinylogous acids Tertiary alcohols Secondary alcohols Cyclic alcohols and derivatives Polyols Oxacyclic compounds Acetals Organic oxides Hydrocarbon derivatives

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Anthraquinone glycoside - Angucycline core - Hydroxyanthraquinone - Naphthalene - Aryl ketone - Quinone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Oxane - Vinylogous acid - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as anthraquinone glycosides. These are organic compounds containing an anthraquinone moiety glycosidically bound to a carbohydrate moiety.

External Descriptors

Not available

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