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)[NH2+])[C@@H](O)[C@@H]2N=C(N)N)O[C@H](C)[C@@]1(O)C=O

InChIKey

InChIKey=GVNYWUGSPXHFQU-APUVXCOVSA-N

Formula

C21H39N7O12

Mass

581.579

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