Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1[C@H](C)O[C@H](NC2=CC(N)=C3C(=O)C4=C(C=C3C2(O)CC2=COC(CC(C)O)=C2)C(=O)C2C([C@H](O)CC3=CC(C)=C(C(=O)OC)C(O)=C23)C4=O)[C@H](OC)[C@@H]1O

InChIKey

InChIKey=NLUOVDZJZHZVMU-ABRSNRIQSA-N

Formula

C41H46N2O14

Mass

790.819

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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 - Phenanthrene - 2-naphthalenecarboxylic acid - 2-naphthalenecarboxylic acid or derivatives - Glycosyl compound - N-glycosyl compound - Salicylic acid or derivatives - Tetralin - 1-hydroxy-4-unsubstituted benzenoid - Cyclohexenone - Phenol - Monosaccharide - Oxane - Furan - Heteroaromatic compound - Vinylogous amide - Vinylogous acid - Methyl ester - Tertiary alcohol - Amino acid or derivatives - Secondary alcohol - Carboxylic acid ester - Ketone - Organoheterocyclic compound - Polyol - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Enamine - Ether - Carbonyl group - Alcohol - Organic oxygen compound - Organic oxide - Primary aliphatic amine - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organonitrogen compound - Primary amine - 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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