Structure Information
Structure

Compound Identification

SMILES

CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@H]1[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](N=C(N)N)[C@@H](O)[C@@H]2N=C(N)N)O[C@@H](CO)[C@]1(O)C=O

InChIKey

InChIKey=OFNXOACBUMGOPC-HZYVHMACSA-N

Formula

C21H39N7O13

Mass

597.579

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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

Amino cyclitol glycoside - Glycosyl compound - O-glycosyl compound - Cyclohexanol - Monosaccharide - Cyclitol or derivatives - Oxane - Cyclic alcohol - Tertiary alcohol - Tetrahydrofuran - 1,2-aminoalcohol - Secondary alcohol - Guanidine - Secondary amine - Secondary aliphatic amine - Polyol - Organic 1,3-dipolar compound - Organoheterocyclic compound - Oxacycle - Acetal - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organonitrogen compound - Primary alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Amine - Aldehyde - Alcohol - Organopnictogen 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

CHEBI:24750 : streptomycins

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