Compound Identification
SMILES
[H][C@](N)(CCCN)CC(O)=NCCC[C@]([H])(N)CC(O)=NCCC[C@]([H])(N)CC(O)=N[C@@]1([H])[C@]([H])(NC2=N[C@@]3([H])[C@]([H])(N2)C(O)=NC[C@@]3([H])O)O[C@]([H])(COC(O)=N)[C@]([H])(O)[C@@]1([H])O
InChIKey
InChIKey=HOIBHXUQBGKGFH-OTQKCRDJSA-N
Formula
C31H58N12O10
Mass
758.879
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Level 5
Glycosyl compounds
- Level 6 Glycosylamines
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Level 5
Glycosyl compounds
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Subclass
Carbohydrates and carbohydrate conjugates
-
Class
Organooxygen compounds
-
Superclass
Organic oxygen compounds
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
Hexoses Imidazopyridines Tetrahydropyridines Oxanes Imidazolines Cyclic carboximidic acids Secondary alcohols Guanidines Oxacyclic compounds Propargyl-type 1,3-dipolar organic compounds Carboximidamides Azacyclic compounds Organopnictogen compounds Monoalkylamines Imines Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Hexose monosaccharide - N-glycosyl compound - Imidazopyridine - Tetrahydropyridine - Monosaccharide - Oxane - Cyclic carboximidic acid - 2-imidazoline - Secondary alcohol - Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Oxacycle - Azacycle - Organoheterocyclic compound - Carboximidic acid - Carboximidic acid derivative - Primary amine - Hydrocarbon derivative - Imine - Organopnictogen compound - Primary aliphatic amine - Organic nitrogen compound - Alcohol - Organonitrogen compound - Amine - Aliphatic heteropolycyclic 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