Structure Information
Structure

Compound Identification

SMILES

[H][C@@]1(N)[C@@]([H])(O)[C@]([H])(O[C@@]2([H])O[C@]([H])(CO[C@@]3([H])O[C@]([H])(CO)[C@@]([H])(O)[C@]([H])(O)[C@]3([H])O[C@@]3([H])O[C@]([H])(COP(O)(=O)OCCN)[C@@]([H])(O)[C@]([H])(O)[C@]3([H])O)[C@@]([H])(O)[C@]([H])(O)[C@]2([H])O)[C@@]([H])(CO)O[C@]1([H])O[C@]1([H])[C@@]([H])(O)[C@]([H])(O)[C@@]([H])(O)[C@@]([H])(O)[C@@]1([H])O

InChIKey

InChIKey=RUOSZMLKJRMVTP-ZXBFNAQLSA-N

Formula

C32H59N2O28P

Mass

950.784

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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

Aminosaccharides - Aminoglycosides

Direct Parent

Aminocyclitol glycosides

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Oligosaccharide phosphate - Oligosaccharide - Amino cyclitol glycoside - Glycosyl compound - O-glycosyl compound - Phosphoethanolamine - Cyclohexanol - Dialkyl phosphate - Cyclitol or derivatives - Alkyl phosphate - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Cyclic alcohol - 1,2-aminoalcohol - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Primary alcohol - Primary amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Amine - Alcohol - Organonitrogen compound - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as aminocyclitol glycosides. These are organic compounds containing an amicocyclitol moiety glycosidically linked to a carbohydrate moiety. There are two major classes of aminoglycosides containing a 2-streptamine core. They are called 4,5- and 4,6-disubstituted 2-deoxystreptamines.

External Descriptors

Not available

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