Structure Information
Structure

Compound Identification

SMILES

NC(=O)C1=CN([C@@H]2O[C@H](COC(=O)C3=CC=CC=C3)[C@@H](OC(=O)C3=CC=CC=C3)[C@H]2OC(=O)C2=CC=CC=C2)C(=C1C(N)=O)[N+]([O-])=O

InChIKey

InChIKey=BMZUEBYCQYTHPX-UQCYUJMQSA-N

Formula

C32H26N4O11

Mass

642.577

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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 - Benzoate ester - Benzoic acid or derivatives - Tricarboxylic acid or derivatives - Nitroaromatic compound - Benzoyl - Pyrrole-3-carboxamide - Pyrrole-3-carboxylic acid or derivatives - Monocyclic benzene moiety - Monosaccharide - Substituted pyrrole - Benzenoid - Oxolane - Vinylogous amide - Pyrrole - Heteroaromatic compound - Carboxylic acid ester - C-nitro compound - Carboxamide group - Organic nitro compound - Primary carboxylic acid amide - Oxacycle - Azacycle - Organoheterocyclic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Organic salt - Organic nitrogen compound - Organic zwitterion - 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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