CCCNC1=NC(N)=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](CO)S1

InChIKey=ZQBUKPZOZDBCII-DJLDLDEBSA-N

C13H20N6O2S

324.4

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Thionucleosides

Not available

Thionucleosides

6-alkylaminopurines Secondary alkylarylamines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Thiolanes Heteroaromatic compounds Secondary alcohols Dialkylthioethers Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine thionucleoside - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - N-substituted imidazole - Imidolactam - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Thiolane - Secondary alcohol - Thioether - Dialkylthioether - Organoheterocyclic compound - Azacycle - Secondary amine - Organic nitrogen compound - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Amine - Alcohol - Aromatic heteropolycyclic compound

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.

Not available