Structure Information
Structure

Compound Identification

SMILES

[H]C(CSC12CC([H])(CC(O)=O)OC([H])(CCC)C1(O)C(=O)C1=C(C=CC=C1O)C2=O)(N=C(C)O)C(O)=O

InChIKey

InChIKey=LBTDZXFVMNOCLO-UHFFFAOYSA-N

Formula

C23H27NO10S

Mass

509.53

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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 - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Cysteine or derivatives - Naphthoquinone - C-glycosyl compound - Glycosyl compound - Alpha-amino acid or derivatives - Naphthalene - Tetralin - Quinone - Aryl alkyl ketone - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Pyranone - Dicarboxylic acid or derivatives - Pyran - Benzenoid - Oxane - Tertiary alcohol - Vinylogous acid - Ketone - Sulfenyl compound - Thioether - Carboximidic acid - Propargyl-type 1,3-dipolar organic compound - Oxacycle - Carboximidic acid derivative - Carboxylic acid derivative - Carboxylic acid - Dialkylthioether - Dialkyl ether - Ether - Organic 1,3-dipolar compound - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organosulfur 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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