Structure Information
Structure

Compound Identification

SMILES

CNC1(C)CC(OC(C)C1OC1CC(OC)C(O)C(C)O1)C1=C(O)C2=C(C=C1)C(=O)C1=CC(=C3C(=O)C=C(OC3=C1C2=O)C1(C)OC1C)C(O)(C1CC(OC)C(O)C(C)O1)C(=O)OC

InChIKey

InChIKey=YRBLXLRNBFXANX-UHFFFAOYSA-N

Formula

C46H57NO17

Mass

895.952

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