Compound Identification
SMILES
NC1=NC=NC2=C1N=CN2C1S[C@@H](CO)C[C@@H]1N=[N+]=[N-]
InChIKey
InChIKey=YLXJDLTWWNTGDI-CGQSYLDTSA-N
Formula
C10H12N8OS
Mass
292.32
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 Azo imides Azo compounds Dialkylthioethers Azacyclic compounds Primary amines Primary alcohols Organic zwitterions Organic salts Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine thionucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Thiolane - Azo compound - Azo imide - Thioether - Organoheterocyclic compound - Azacycle - Dialkylthioether - Primary amine - Organonitrogen compound - Amine - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organooxygen compound - Primary alcohol - Organic oxygen compound - Organic zwitterion - Organic salt - 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