Structure Information
Structure

Compound Identification

SMILES

COC1=CC(=O)C2=C(O)C3=C(C[C@@H]4[C@@H](O[C@H]5CC[C@H](O[C@H]6CC[C@H](O[C@H]7CC[C@H](O[C@H]8CC[C@H](OC(=O)C(C)(C)C(O)=O)[C@H](C)O8)[C@H](C)O7)[C@H](C)O6)[C@@H](C)O5)C(=O)C(C(C)=O)=C(O)[C@]4(O[C@H]4CC[C@H](O[C@H]5CC[C@H](O)[C@@H](C)O5)[C@@H](C)O4)C3=O)C=C2C1=O

InChIKey

InChIKey=DTTQURMKQUWCNN-ZVSUTAIVSA-N

Formula

C62H82O25

Mass

1227.313

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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

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Anthraquinone glycoside - Naphthalene - Tetralin - Quinone - Aryl ketone - Aryl alkyl ketone - 1-hydroxy-4-unsubstituted benzenoid - Cyclohexenone - Dicarboxylic acid or derivatives - Oxane - Vinylogous ester - Vinylogous acid - Secondary alcohol - Cyclic ketone - Ketone - Carboxylic acid ester - Acetal - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Enol - Carboxylic acid - Alcohol - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Aldehyde - Organooxygen compound - 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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