Compound Identification
SMILES
CCC1=CN([C@@H]2S[C@H](CO)[C@@H](O)[C@@H]2F)C(=O)NC1=O
InChIKey
InChIKey=IFVZEUHPOPNVSS-IBCQBUCCSA-N
Formula
C11H15FN2O4S
Mass
290.31
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
Pyrimidones Hydropyrimidines Heteroaromatic compounds Vinylogous amides Thiolanes Lactams Fluorohydrins Ureas Secondary alcohols Azacyclic compounds Dialkylthioethers Primary alcohols Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine thionucleoside - Pyrimidone - Hydropyrimidine - Pyrimidine - Thiolane - Vinylogous amide - Heteroaromatic compound - Fluorohydrin - Halohydrin - Lactam - Urea - Secondary alcohol - Azacycle - Organoheterocyclic compound - Dialkylthioether - Thioether - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Hydrocarbon derivative - Organic nitrogen compound - Alkyl halide - Alkyl fluoride - Organic oxygen compound - Organic oxide - Alcohol - 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