Compound Identification
SMILES
OCC1OC(C(O)C1O)N1C=NC2=C1N=CN=C2NCC1C2=CC=CC=C2OC2=CC=CC=C12
InChIKey
InChIKey=WMMRZGKUFUEPTA-UHFFFAOYSA-N
Formula
C24H23N5O5
Mass
461.478
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
Xanthenes 6-alkylaminopurines Diarylethers Glycosylamines Pentoses Secondary alkylarylamines Aminopyrimidines and derivatives Benzenoids Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Dibenzopyran - Xanthene - Diaryl ether - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Benzopyran - Pentose monosaccharide - 1-benzopyran - Purine - Imidazopyrimidine - Secondary aliphatic/aromatic amine - Aminopyrimidine - Imidolactam - Benzenoid - Pyrimidine - Monosaccharide - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - 1,2-diol - Ether - Secondary amine - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Primary alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Amine - 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