Compound Identification
SMILES
NC1=NC2=C(N=CN2C2S[C@H](CO)[C@@H](O)[C@@H]2O)C(N)=N1
InChIKey
InChIKey=NNQXXWXKJFKCQU-PTSYZVBVSA-N
Formula
C10H14N6O3S
Mass
298.32
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
- Subclass Thionucleosides
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Class
Nucleoside and nucleotide analogues
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Thionucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Thionucleosides
Alternative Parents
6-aminopurines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Thiolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Dialkylthioethers Azacyclic compounds Primary amines Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine thionucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Thiolane - Heteroaromatic compound - Azole - Imidazole - Secondary alcohol - 1,2-diol - Azacycle - Thioether - Organoheterocyclic compound - Dialkylthioether - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Primary alcohol - Organic oxygen compound - Amine - Primary amine - Alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as thionucleosides. These are nucleoside analogues that contain a thiolane or a thietane that is 1,3-disubstituted with a hydroxyl group and pyrimidine or purine base, at the 1- and 3-position, respectively.
External Descriptors
Not available