Structure Information
Structure

Compound Identification

SMILES

[H][C@](N)(CCCN)CC(O)=NCCC[C@]([H])(N)CC(O)=NCCC[C@]([H])(N)CC(O)=N[C@@]1([H])[C@]([H])(NC2=N[C@@]3([H])[C@]([H])(N2)C(O)=NC[C@@]3([H])O)O[C@]([H])(COC(O)=N)[C@]([H])(O)[C@@]1([H])O

InChIKey

InChIKey=HOIBHXUQBGKGFH-OTQKCRDJSA-N

Formula

C31H58N12O10

Mass

758.879

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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

Aliphatic heteropolycyclic compounds

Substituents

Hexose monosaccharide - N-glycosyl compound - Imidazopyridine - Tetrahydropyridine - Monosaccharide - Oxane - Cyclic carboximidic acid - 2-imidazoline - Secondary alcohol - Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Oxacycle - Azacycle - Organoheterocyclic compound - Carboximidic acid - Carboximidic acid derivative - Primary amine - Hydrocarbon derivative - Imine - Organopnictogen compound - Primary aliphatic amine - Organic nitrogen compound - Alcohol - Organonitrogen compound - Amine - Aliphatic heteropolycyclic 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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