Compound Identification
SMILES
OC[C@H]1S[C@@H](C[C@@H]1N=[N+]=[N-])N1C=C(Cl)C(=O)NC1=O
InChIKey
InChIKey=FYDAAGUWNIHUEX-XVMARJQXSA-N
Formula
C9H10ClN5O3S
Mass
303.72
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 Halopyrimidines Aryl chlorides Hydropyrimidines Vinylogous amides Thiolanes Heteroaromatic compounds Ureas Azo compounds Azo imides Lactams Azacyclic compounds Dialkylthioethers Organic salts Primary alcohols Organic zwitterions Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine thionucleoside - Halopyrimidine - Pyrimidone - Aryl chloride - Aryl halide - Hydropyrimidine - Pyrimidine - Vinylogous amide - Heteroaromatic compound - Thiolane - Urea - Azo compound - Azo imide - Lactam - Dialkylthioether - Azacycle - Organoheterocyclic compound - Thioether - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Primary alcohol - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic zwitterion - Organic oxide - Organic salt - 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