Compound Identification
SMILES
OC[C@H]1OC([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NCC1=NC=C(O)C=C1
InChIKey
InChIKey=IRZNDKKKFMEHTG-AARXTDBFSA-N
Formula
C16H18N6O5
Mass
374.357
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 2-pyridylmethylamines Aminopyrimidines and derivatives Hydroxypyridines N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Amines Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - 6-alkylaminopurine - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - 6-aminopurine - Imidazopyrimidine - Purine - 2-pyridylmethylamine - Aminopyrimidine - Hydroxypyridine - Monosaccharide - Imidolactam - N-substituted imidazole - Pyridine - Pyrimidine - Heteroaromatic compound - Oxolane - Azole - Imidazole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - 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