Compound Identification
SMILES
NC1=NC(=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C1=CC=CC=C1
InChIKey
InChIKey=RHYBPJRGJJLRQM-UBEDBUPSSA-N
Formula
C16H17N5O4
Mass
343.343
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 Pentoses Aminopyrimidines and derivatives Benzene and substituted derivatives Imidolactams N-substituted imidazoles Heteroaromatic compounds Tetrahydrofurans Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Primary amines Organopnictogen compounds Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Imidolactam - Azole - Tetrahydrofuran - Imidazole - Heteroaromatic compound - Secondary alcohol - Azacycle - Oxacycle - Organoheterocyclic compound - Primary amine - Alcohol - Amine - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - 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