Structure Information
Structure

Compound Identification

SMILES

COC(=O)C12OCC34C1C(OC(=O)C=C(C)C)C(=O)OC3C=C1C(C)C(=O)C(OC3OC(CO)C(O)C(O)C3O)=CC1(C)C4C(O)C2O

InChIKey

InChIKey=FQLFRZWZGRZRKR-UHFFFAOYSA-N

Formula

C32H40O16

Mass

680.656

Export to:

JSON SDF CSV

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

Aliphatic heteropolycyclic compounds

Substituents

Naphthopyranone glycoside - C-20 quassinoid skeleton - Quassinoid - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Naphthalene - Tricarboxylic acid or derivatives - Furopyran - Cyclohexenone - Pyranone - Oxepane - Delta_valerolactone - Fatty acid ester - Delta valerolactone - Beta-hydroxy acid - Fatty acyl - Pyran - Oxane - Monosaccharide - Hydroxy acid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Methyl ester - Tetrahydrofuran - Furan - Cyclic alcohol - Cyclic ketone - Secondary alcohol - Lactone - Ketone - Carboxylic acid ester - Oxacycle - Polyol - Ether - Dialkyl ether - Carboxylic acid derivative - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic 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

Previous Back Next