Compound Identification
SMILES
NC1=NC(=O)N(C=C1F)[C@@H]1S[C@H](CO)[C@@H](O)[C@@H]1O
InChIKey
InChIKey=QDVOFRWTPUEFTR-MNCSTQPFSA-N
Formula
C9H12FN3O4S
Mass
277.27
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
Pyrimidones Aminopyrimidines and derivatives Halopyrimidines Aryl fluorides Imidolactams Hydropyrimidines Thiolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Azacyclic compounds Dialkylthioethers Primary alcohols Primary amines Organofluorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine thionucleoside - Aminopyrimidine - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - Pyrimidine - Imidolactam - Heteroaromatic compound - Thiolane - Secondary alcohol - 1,2-diol - Thioether - Azacycle - Organoheterocyclic compound - Dialkylthioether - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Amine - Organic oxygen compound - Alcohol - Primary alcohol - Primary amine - Organic nitrogen compound - Organic oxide - Aromatic heteromonocyclic 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