Compound Identification
SMILES
OC[C@@H]1O[C@H]([C@@H](O)[C@H]1O)N1C=NC2=C1N=CN=C2SCC1=CC=CC=C1
InChIKey
InChIKey=OMJRXFOHHLLDFR-PLNCSYRRSA-N
Formula
C17H18N4O4S
Mass
374.42
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-thiopurines Pentoses Alkylarylthioethers Pyrimidines and pyrimidine derivatives N-substituted imidazoles Benzene and substituted derivatives Oxolanes Heteroaromatic compounds Secondary alcohols Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organonitrogen compounds Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 6-thiopurine - Imidazopyrimidine - Purine - Aryl thioether - Alkylarylthioether - Benzenoid - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Oxolane - Heteroaromatic compound - Secondary alcohol - Organoheterocyclic compound - Thioether - Sulfenyl compound - Oxacycle - Azacycle - Alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - 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