Compound Identification
SMILES
NC1=NC(N\N=C\C=C\C2=CC=CO2)=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
InChIKey
InChIKey=WXRDMKRQDSHLPI-RNRNVXBSSA-N
Formula
C17H19N7O5
Mass
401.383
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-aminopurines Pentoses Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Furans Heteroaromatic compounds Oxolanes Secondary alcohols 1,2-diols Hydrazones Azacyclic compounds Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Monosaccharide - Imidolactam - Pyrimidine - Imidazole - Furan - Heteroaromatic compound - Oxolane - Azole - 1,2-diol - Secondary alcohol - Hydrazone - Organoheterocyclic compound - Azacycle - Oxacycle - Primary alcohol - Primary amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Alcohol - Organooxygen compound - Organonitrogen 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