Structure Information
Structure

Compound Identification

SMILES

COC1CC(OC2C(C)OC(CC2(C)N(C)C)C2=C(O)C3=C(C=C2)C(=O)C2=CC(=C4C(=O)C=C(OC4=C2C3=O)C2(C)OC2C)C(O)(C2CC(OC)C(O)C(C)O2)C(=O)OC)OC(C)C1O

InChIKey

InChIKey=CSPDCSMLEJFUJJ-UHFFFAOYSA-N

Formula

C47H59NO17

Mass

909.979

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