Compound Identification
SMILES
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NC(N1N=NC2=CC=CC=C12)C1=CC=CO1
InChIKey
InChIKey=KWRUWPWFLOJKMG-BFFDMINNSA-N
Formula
C21H20N8O5
Mass
464.442
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
6-alkylaminopurines Glycosylamines Pentoses Benzotriazoles Benzenoids Pyrimidines and pyrimidine derivatives Imidolactams N-substituted imidazoles Triazoles Heteroaromatic compounds Furans Oxolanes Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organonitrogen compounds Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - Pentose monosaccharide - Benzotriazole - Imidazopyrimidine - Purine - Benzenoid - Pyrimidine - Imidolactam - N-substituted imidazole - Monosaccharide - 1,2,3-triazole - Triazole - Azole - Heteroaromatic compound - Oxolane - Furan - Imidazole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Primary alcohol - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Alcohol - Organooxygen compound - Hydrocarbon derivative - 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