Compound Identification
SMILES
CNC1=NC=NC2=C1N=CN2[C@@H]1S[C@H](CO)C[C@@H]1N=[N+]=[N-]
InChIKey
InChIKey=JEDAWZPZTLQCLS-OKTBNZSVSA-N
Formula
C11H14N8OS
Mass
306.35
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
- Subclass Thionucleosides
-
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-alkylaminopurines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Thiolanes Heteroaromatic compounds Azo imides Azo compounds Dialkylthioethers Azacyclic compounds Primary alcohols Organic zwitterions Organic salts Hydrocarbon derivatives Amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine thionucleoside - 6-alkylaminopurine - 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 alcohol - Amine - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic salt - Organic zwitterion - 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