Structure Information
Structure

Compound Identification

SMILES

COC1CC(OC2C(C)OC(CC2(C)N)C2=C(O)C3=C(C=C2)C(=O)C2=CC(=C4C(=O)C=C(OC4=C2C3=O)C2(C)OC2C)C(O)(C2OC(C)C(O)C(OC)C2O)C(=O)OC)OC(C)C1O

InChIKey

InChIKey=HUERDIYXSZKKMF-UHFFFAOYSA-N

Formula

C45H55NO18

Mass

897.924

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Naphthopyrans

Subclass

Naphthopyranones

Intermediate Tree Nodes

Not available

Direct Parent

Naphthopyranone glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Naphthopyranone glycoside - 9,10-anthraquinone - Anthraquinone - Anthracene - O-glycosyl compound - Chromone - Glycosyl compound - Benzopyran - 1-benzopyran - Aryl ketone - Aralkylamine - Pyranone - 1-hydroxy-4-unsubstituted benzenoid - Oxane - Benzenoid - Monosaccharide - Pyran - Methyl ester - Tertiary alcohol - Heteroaromatic compound - Vinylogous acid - Amino acid or derivatives - Carboxylic acid ester - Ketone - Secondary alcohol - Acetal - Carboxylic acid derivative - Dialkyl ether - Oxirane - Ether - Oxacycle - Monocarboxylic acid or derivatives - Primary amine - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Amine - Primary aliphatic amine - Organopnictogen compound - Aromatic alcohol - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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