Compound Identification
SMILES
C[C@]1(O)[C@@H](O)[C@H](COP(N)(=O)OP(O)(=O)OP(O)(O)=O)O[C@@H]1N1C=NC2=C1NC(N)=NC2=O
InChIKey
InChIKey=RSJUCGJZGPJXCG-VWZNVGQPSA-N
Formula
C11H19N6O13P3
Mass
536.223
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
-
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-oxopurines Hypoxanthines Pentoses Aminopyrimidines and derivatives Pyrimidones N-substituted imidazoles Organic phosphoramides Phosphate esters Vinylogous amides Heteroaromatic compounds Oxolanes Tertiary alcohols 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-glycosyl compound - 6-oxopurine - Hypoxanthine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Organic phosphoric acid amide - Phosphoric acid ester - Pyrimidine - Imidazole - Vinylogous amide - Azole - Oxolane - Tertiary alcohol - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Alcohol - Amine - Primary amine - Hydrocarbon derivative - 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