Compound Identification
SMILES
OC[C@H]1S[C@@H]([C@@H](O)[C@@H]1O)N1C=C(\C=C\Cl)C(=O)NC1=O
InChIKey
InChIKey=SBDDHCFEHJZNAR-WJDCWECUSA-N
Formula
C11H13ClN2O5S
Mass
320.74
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 Vinylogous amides Thiolanes Heteroaromatic compounds Ureas Secondary alcohols Lactams Vinyl chlorides Azacyclic compounds Chloroalkenes Dialkylthioethers Hydrocarbon derivatives Organic oxides Organochlorides Organonitrogen compounds Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine thionucleoside - Pyrimidone - Hydropyrimidine - Pyrimidine - Heteroaromatic compound - Thiolane - Vinylogous amide - Lactam - Secondary alcohol - Urea - Azacycle - Thioether - Chloroalkene - Haloalkene - Vinyl chloride - Vinyl halide - Organoheterocyclic compound - Dialkylthioether - Hydrocarbon derivative - Organic oxide - Primary alcohol - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - 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