Compound Identification
SMILES
CC1=CC=CC=C1CN(C1CCCC1)C1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
InChIKey
InChIKey=UZKIDIVSLQOZAF-ZDXOVATRSA-N
Formula
C23H29N5O4
Mass
439.516
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 Dialkylarylamines Aminopyrimidines and derivatives Toluenes N-substituted imidazoles Imidolactams Heteroaromatic compounds Oxolanes Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Dialkylarylamine - Benzylamine - Aminopyrimidine - Toluene - Monocyclic benzene moiety - Imidolactam - Benzenoid - Monosaccharide - N-substituted imidazole - Pyrimidine - Oxolane - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Amine - Alcohol - Primary alcohol - 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