Structure Information
Structure

Compound Identification

SMILES

CCCC1CC2=C(C(=O)O1)C(O)=C1C(=C2)C(O)C(O)C2=C(OC)C3=C(C(O)=C12)C(=O)C1=C(O3)C=CC(O[C@H]2CC(O[C@H]3C[C@@H](O)C(O[C@H]4C[C@@H](OC)[C@H](O)[C@@H](C)O4)[C@@H](C)O3)[C@H](O)[C@@H](C)O2)=C1O

InChIKey

InChIKey=ZLVZEEVFLRAYLU-YUASZBMKSA-N

Formula

C47H56O20

Mass

940.945

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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 - Xanthone - Dibenzopyran - Phenanthrene - Xanthene - Chromone - Disaccharide - Glycosyl compound - 1-naphthol - O-glycosyl compound - Benzopyran - Isochromane - Naphthalene - 2-benzopyran - 1-benzopyran - Anisole - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Pyranone - Benzenoid - Oxane - Pyran - Vinylogous acid - Heteroaromatic compound - Carboxylic acid ester - Lactone - Secondary alcohol - Ether - Monocarboxylic acid or derivatives - Dialkyl ether - Oxacycle - Polyol - Carboxylic acid derivative - Acetal - Organooxygen compound - Alcohol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - 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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