Compound Identification
SMILES
CC(Cl)C1=CN([C@@H]2S[C@H](CO)[C@@H](O)[C@H]2O)C(=O)NC1=O
InChIKey
InChIKey=RCOUGIWHGJWRQZ-XFBDIIGESA-N
Formula
C11H15ClN2O5S
Mass
322.76
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 1,2-diols Ureas Secondary alcohols Dialkylthioethers Azacyclic compounds Primary alcohols Organonitrogen compounds Organochlorides Organic oxides Alkyl chlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine thionucleoside - Pyrimidone - Hydropyrimidine - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Thiolane - 1,2-diol - Lactam - Secondary alcohol - Urea - Azacycle - Organoheterocyclic compound - Thioether - Dialkylthioether - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Alcohol - Alkyl chloride - Alkyl halide - 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