Compound Identification
SMILES
CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NC(C)=O
InChIKey
InChIKey=IFPLJRYXTIQPPU-AEISUSGSSA-N
Formula
C14H18N6O5
Mass
350.335
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 N-acetylarylamines Purines and purine derivatives N-substituted imidazoles Imidolactams Pyrimidines and pyrimidine derivatives Acetamides Oxolanes Heteroaromatic compounds 1,2-diols Secondary carboxylic acid amides Secondary alcohols Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Imidazopyrimidine - N-acetylarylamine - Purine - N-arylamide - Imidolactam - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Azole - Acetamide - Imidazole - Oxolane - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - 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