Structure Information
Structure

Compound Identification

SMILES

C[NH2+][C@@H]1[C@@H](O)[C@H](O[C@H]2[C@H]([NH3+])C[C@H]([NH3+])[C@@H](O[C@H]3OC(C[NH3+])=CC[C@H]3[NH3+])[C@@H]2O)OC[C@]1(C)O

InChIKey

InChIKey=URWAJWIAIPFPJE-RPMBBHDKSA-S

Formula

C19H42N5O7

Mass

452.57

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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 - Aminocyclitol or derivatives - Cyclohexylamine - Cyclohexanol - Oxane - Monosaccharide - Cyclitol or derivatives - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - 1,2-aminoalcohol - Oxacycle - Organoheterocyclic compound - Secondary amine - Secondary aliphatic amine - Acetal - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - 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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