Compound Identification
SMILES
CC(CNC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@@]1(C)O)C1=CC=CC=C1
InChIKey
InChIKey=QZHLPBWBMZTMIY-GFMOLVTGSA-N
Formula
C20H25N5O4
Mass
399.451
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 Aminopyrimidines and derivatives Benzene and substituted derivatives Imidolactams N-substituted imidazoles Heteroaromatic compounds Tertiary alcohols Oxolanes Secondary alcohols Azacyclic compounds Oxacyclic compounds Amines 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 - Aminopyrimidine - Monocyclic benzene moiety - Imidolactam - Monosaccharide - N-substituted imidazole - Benzenoid - Pyrimidine - Heteroaromatic compound - Tertiary alcohol - Oxolane - Azole - Imidazole - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Primary alcohol - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - 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