Compound Identification
SMILES
NC1=NC(NCC2CCCO2)=NC2=C1N=CN2C1OC(CO)[C@H](O)[C@@H]1O
InChIKey
InChIKey=CEXDWZVFPCSZCQ-PYUWGYSASA-N
Formula
C15H22N6O5
Mass
366.378
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 Secondary alkylarylamines Aminopyrimidines and derivatives Imidolactams Monosaccharides N-substituted imidazoles Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Dialkyl ethers Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - N-substituted imidazole - Monosaccharide - Imidolactam - Pyrimidine - Oxolane - Heteroaromatic compound - Imidazole - Azole - 1,2-diol - Secondary alcohol - Oxacycle - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Secondary amine - Amine - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Primary 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