Compound Identification
SMILES
CN(CC1=CC=CC=C1)CC1=C2N=CN([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)C2=NC=N1
InChIKey
InChIKey=PTTZAWXQBYNYMK-KLICCBINSA-N
Formula
C19H23N5O4
Mass
385.424
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 Pentoses Purines and purine derivatives Phenylmethylamines Benzylamines Aralkylamines Pyrimidines and pyrimidine derivatives N-substituted imidazoles Oxolanes Heteroaromatic compounds Trialkylamines Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Imidazopyrimidine - Purine - Benzylamine - Phenylmethylamine - Aralkylamine - Benzenoid - Pyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Azole - Heteroaromatic compound - Oxolane - Imidazole - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-diol - Azacycle - Organoheterocyclic compound - Oxacycle - Organic oxygen compound - Organic nitrogen compound - Alcohol - Primary alcohol - Amine - Organooxygen compound - Hydrocarbon derivative - 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