Structure Information
Structure

Compound Identification

SMILES

CCC[C@H]1O[C@H](CC(N)=O)C[C@]2(S[C@]34C[C@@H](CC(N)=O)O[C@H](CCC)[C@]3(O)C(=O)C3=C(O)C=C(OC)C=C3C4=O)C(=O)C3=CC(OC)=CC(O)=C3C(=O)[C@@]12O

InChIKey

InChIKey=BHFIVAGXJHEBFL-IKLOEFKXSA-N

Formula

C38H44N2O14S

Mass

784.83

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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 - Naphthoquinone - C-glycosyl compound - Glycosyl compound - Naphthalene - Tetralin - Anisole - Phenol ether - Quinone - Aryl ketone - Aryl alkyl ketone - 1-hydroxy-4-unsubstituted benzenoid - Pyranone - Phenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Pyran - Oxane - Vinylogous acid - Tertiary alcohol - Carboxamide group - Ketone - Primary carboxylic acid amide - Oxacycle - Sulfenyl compound - Dialkylthioether - Thioether - Carboxylic acid derivative - Dialkyl ether - Ether - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Alcohol - Organosulfur compound - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen 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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