Compound Identification
SMILES
COCOCC1=NC(=O)C2=C(N1)N(C=N2)[C@H]1O[C@@H](CO)[C@H](O)[C@@H]1O
InChIKey
InChIKey=CJNXQLOSSRXGII-VHMYRRENSA-N
Formula
C13H18N4O7
Mass
342.308
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Purine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Purine nucleosides
Alternative Parents
Glycosylamines 6-oxopurines Hypoxanthines Pentoses Pyrimidones N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxolanes Secondary alcohols Azacyclic compounds Acetals Oxacyclic compounds Organic oxides Primary alcohols Hydrocarbon derivatives Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Pentose monosaccharide - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Pyrimidone - N-substituted imidazole - Monosaccharide - Pyrimidine - Oxolane - Vinylogous amide - Imidazole - Heteroaromatic compound - Azole - Secondary alcohol - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors
Not available