Compound Identification
SMILES
CS[13C]1=[15N]C(=O)C2=C([15NH]1)N(C=N2)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
InChIKey
InChIKey=UKKPPYZMRPWXAX-FMOQMKROSA-N
Formula
C11H14N4O5S
Mass
317.29
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 Pentoses Alkylarylthioethers Pyrimidones N-substituted imidazoles Oxolanes Heteroaromatic compounds Vinylogous amides 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Sulfenyl compounds Primary alcohols Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Pentose monosaccharide - Purinone - Imidazopyrimidine - Purine - Aryl thioether - Alkylarylthioether - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Vinylogous amide - Imidazole - Oxolane - Heteroaromatic compound - Azole - 1,2-diol - Secondary alcohol - Oxacycle - Thioether - Sulfenyl compound - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - Organic oxygen compound - Organosulfur compound - Hydrocarbon derivative - Alcohol - 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