Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1O[C@H](C[C@H](NC(=O)C(F)(F)F)[C@@H]1O)O[C@H]1C[C@](CC2=C(O)C3=C(C(O)=C12)C(=O)C1=C(N(C)C2=CC=CC=C12)C3=O)(O[C@H]1C[C@H](NC(=O)C(F)(F)F)[C@H](O)[C@H](C)O1)C(C)=O

InChIKey

InChIKey=HKHSDJQKACEFCL-SBNCUPENSA-N

Formula

C39H39F6N3O13

Mass

871.739

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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 - Carbazole - Indolecarboxylic acid derivative - O-glycosyl compound - Glycosyl compound - N-alkylindole - Naphthalene - Tetralin - Indole - Indole or derivatives - Aryl ketone - N-methylpyrrole - Monosaccharide - Oxane - Substituted pyrrole - Heteroaromatic compound - Vinylogous amide - Vinylogous acid - Pyrrole - Ketone - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Alkyl fluoride - Aldehyde - Hydrocarbon derivative - Organic oxide - Alcohol - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen 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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