Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1[C@@H](O)[C@@H](C)O[C@H](O[C@H]2[C@H](OC3=CC=CC4=C3C3=C5C6C(C(C)=CC=C6OC(=O)C5=C4O)C(=O)O3)O[C@H](C)[C@H](O)[C@]2(C)O)[C@@H]1N(C)C

InChIKey

InChIKey=ITMIYTCICAQJHX-ZUYDTEIGSA-N

Formula

C35H41NO13

Mass

683.707

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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 - Aminoglycoside core - Phenolic glycoside - 3,4-dihydrocoumarin - Disaccharide - Glycosyl compound - 1-naphthol - O-glycosyl compound - Chromane - Benzopyran - Isochromane - Naphthalene - 2-benzopyran - 1-benzopyran - Amino saccharide - Pyranone - Pyran - Dicarboxylic acid or derivatives - Oxane - Benzenoid - Tertiary alcohol - Enol ester - Vinylogous acid - Carboxylic acid ester - Secondary alcohol - Tertiary amine - Lactone - Tertiary aliphatic amine - Amino acid or derivatives - Ether - Dialkyl ether - Acetal - Oxacycle - Carboxylic acid derivative - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Alcohol - Organonitrogen 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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