Structure Information
Structure

Compound Identification

SMILES

CC(=O)OCC1OC(C(NC(=O)OCC2=CC=CC=C2)C(OC(C)=O)C1OC(C)=O)N1C=CC(NC(=O)C2=CC=C(C=C2)[N+]([O-])=O)=NC1=O

InChIKey

InChIKey=RDGMOUGHZCVQNJ-UHFFFAOYSA-N

Formula

C31H31N5O13

Mass

681.611

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Glycosyl compounds

Direct Parent

Glycosylamines

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

N-glycosyl compound - Benzyloxycarbonyl - Benzamide - Benzoic acid or derivatives - Nitrobenzene - Tricarboxylic acid or derivatives - Nitroaromatic compound - Benzoyl - Pyrimidone - Monocyclic benzene moiety - Imidolactam - Hydropyrimidine - Monosaccharide - Benzenoid - Oxane - Pyrimidine - Heteroaromatic compound - Carbamic acid ester - Organic nitro compound - Carboxamide group - Carboxylic acid ester - C-nitro compound - Carbonic acid derivative - Secondary carboxylic acid amide - Oxacycle - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Carboxylic acid derivative - Organic oxoazanium - Azacycle - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organic zwitterion - Hydrocarbon derivative - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).

External Descriptors

Not available

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