Compound Identification
SMILES
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C(CN3CCSC3)N=CN=C12
InChIKey
InChIKey=FBLZRACPUXSACL-XIDUGBJDSA-N
Formula
C14H19N5O4S
Mass
353.4
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 N-substituted imidazoles Pyrimidines and pyrimidine derivatives Heteroaromatic compounds Thiazolidines Oxolanes 1,2-diols Tertiary amines Secondary alcohols Dialkylthioethers Oxacyclic compounds Azacyclic compounds Thiohemiaminal derivatives Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Imidazopyrimidine - Purine - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Thiazolidine - Oxolane - Heteroaromatic compound - 1,2-diol - Tertiary amine - Secondary alcohol - Azacycle - Thioether - Hemithioaminal - Oxacycle - Dialkylthioether - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - Amine - 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