Compound Identification
SMILES
[H][C@@](O)(CO)[C@@]1([H])O[C@]([H])(OC2([H])[C@@]([H])(O)[C@@]([H])(CO)O[C@@]([H])(O[C@@]3([H])[C@]([H])(O)[C@@]([H])(CO)O[C@]([H])(O[C@@]4([H])[C@]([H])(O)[C@@]([H])(CO)O[C@@]([H])(O)[C@]4([H])N=C(C)O)[C@]3([H])N=C(C)O)[C@]2([H])O)[C@@]([H])(O)[C@@]([H])(O[C@@]2([H])O[C@]([H])(C)[C@@]([H])(O)[C@]([H])(N=CO)[C@@]2([H])O)[C@]1([H])O
InChIKey
InChIKey=CUACRVDCMIPEPH-HTXBJVSWSA-N
Formula
C36H61N3O26
Mass
951.879
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
- Level 5 Oligosaccharides
-
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
Not available
Direct Parent
Oligosaccharides
Alternative Parents
N-acyl-alpha-hexosamines O-glycosyl compounds Oxanes Secondary alcohols Hemiacetals Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Carboximidic acids Acetals Primary alcohols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Oligosaccharide - N-acyl-alpha-hexosamine - Glycosyl compound - O-glycosyl compound - Oxane - Hemiacetal - Secondary alcohol - Acetal - Carboximidic acid - Carboximidic acid derivative - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Organic nitrogen compound - Primary alcohol - Organopnictogen compound - Aliphatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.
External Descriptors
Not available