Compound Identification
SMILES
CC1=CC(CNC2=NC(N)=NC3=C2N=CN3C2OC(CO)[C@H](O)[C@@H]2O)=CC=C1
InChIKey
InChIKey=QWHGNBWUFRSORG-XQZPOBRMSA-N
Formula
C18H22N6O4
Mass
386.412
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 Benzylamines Toluenes Secondary alkylarylamines Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Benzylamine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Toluene - Monocyclic benzene moiety - Monosaccharide - Pyrimidine - Benzenoid - N-substituted imidazole - Imidolactam - Heteroaromatic compound - Azole - Imidazole - Oxolane - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Secondary amine - Azacycle - Oxacycle - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organooxygen compound - Amine - Primary amine - Primary alcohol - 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