Compound Identification
SMILES
COCCO[C@@H]1[C@@H](O)[C@@H](CO)O[C@H]1N1C=NC2=C1NC(N)=NC2=O
InChIKey
InChIKey=DLLBJSLIKOKFHE-IQEPQDSISA-N
Formula
C13H19N5O6
Mass
341.324
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-oxopurines Hypoxanthines Aminopyrimidines and derivatives Pyrimidones Monosaccharides N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxolanes Secondary alcohols Dialkyl ethers Azacyclic compounds Oxacyclic compounds Organic oxides Primary alcohols Hydrocarbon derivatives Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Vinylogous amide - Secondary alcohol - Dialkyl ether - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Amine - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Primary alcohol - Primary amine - 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