Compound Identification
SMILES
OC[C@H]1C[C@H](N=[N+]=[N-])[C@@H](S1)N1C=NC2=C1NC=NC2=O
InChIKey
InChIKey=LYIMYZMUCXHUKQ-GOZTUDAPSA-N
Formula
C10H11N7O2S
Mass
293.31
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
6-oxopurines Hypoxanthines Pyrimidones N-substituted imidazoles Vinylogous amides Thiolanes Heteroaromatic compounds Azo compounds Azo imides Azacyclic compounds Dialkylthioethers Primary alcohols Organic salts Organic zwitterions Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine thionucleoside - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Pyrimidone - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Thiolane - Azo compound - Azo imide - Organoheterocyclic compound - Azacycle - Dialkylthioether - Thioether - Organic salt - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Primary alcohol - Organic zwitterion - Aromatic heteropolycyclic 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