Compound Identification
SMILES
CC1=CC=C(CSC2=NC=NC3=C2N=CN3[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=C1
InChIKey
InChIKey=MBYQFUKERMUKDQ-SCFUHWHPSA-N
Formula
C18H20N4O4S
Mass
388.44
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 Toluenes Alkylarylthioethers Pyrimidines and pyrimidine derivatives N-substituted imidazoles Heteroaromatic compounds Oxolanes Secondary alcohols Sulfenyl compounds Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 6-thiopurine - Imidazopyrimidine - Purine - Aryl thioether - Toluene - Alkylarylthioether - Benzenoid - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Oxolane - Heteroaromatic compound - Secondary alcohol - Sulfenyl compound - Thioether - Organoheterocyclic compound - Oxacycle - Azacycle - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - 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