Compound Identification
SMILES
NS(=O)C1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
InChIKey
InChIKey=CVUBOZOQGQKAPH-JOILOJCLSA-N
Formula
C10H13N5O5S
Mass
315.3
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 Pentoses Purines and purine derivatives Pyrimidines and pyrimidine derivatives N-substituted imidazoles Oxolanes Heteroaromatic compounds Sulfinic acid amides Secondary alcohols 1,2-diols Aminosulfinyl compounds Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Imidazopyrimidine - Purine - Monosaccharide - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Oxolane - Azole - Imidazole - Sulfinic acid derivative - Sulfinic acid amide - Secondary alcohol - Aminosulfinyl compound - 1,2-diol - Sulfinyl compound - Azacycle - Oxacycle - Organoheterocyclic compound - Primary alcohol - Alcohol - Organonitrogen compound - Organic oxide - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Organosulfur compound - Hydrocarbon derivative - 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