Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](NC2=CC=C(C=C2)[Sb](O)(=O)O[Sb](=O)(O[Sb]([O-])(=O)C2=CC=C(N[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2)C2=CC=C(N[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=OGVJZMYPGSOHDS-VZUYEAPTSA-M

Formula

C36H49N3O22Sb3

Mass

1241.068

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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 - Phenylalkylamine - Aniline or substituted anilines - Monocyclic benzene moiety - Metal aryl - Monosaccharide - Oxane - Benzenoid - Organic antimony salt - Secondary alcohol - Oxacycle - Polyol - Organic metal salt - Organic metalloid salt - Organoheterocyclic compound - Amine - Alcohol - Organonitrogen compound - Organometallic compound - Organoantimony compound - Organic metalloid moeity - Hydrocarbon derivative - Primary alcohol - Organic nitrogen compound - Organic oxide - Organic anion - 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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