Compound Identification
SMILES
[Na+].CP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N
InChIKey
InChIKey=ITRXRIZMQUFQPK-YCSZXMBFSA-M
Formula
C11H15N5NaO6P
Mass
367.234
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
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Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
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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
6-aminopurines Pentoses Aminopyrimidines and derivatives Phosphonic acid esters Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes Organic phosphonic acids Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Primary amines Organic oxides Hydrocarbon derivatives Organic sodium salts Organic zwitterions Organophosphorus compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Phosphonic acid ester - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Organophosphonic acid - Organophosphonic acid derivative - Oxolane - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Organic zwitterion - Organic nitrogen compound - Organic oxide - Organic salt - Organic sodium salt - Hydrocarbon derivative - Organonitrogen compound - Alcohol - Primary amine - Organophosphorus compound - Amine - Aromatic 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