NC1=NC(Cl)=NC2=C1N=CN2[C@@H]1C[C@H](O)[C@H](CO)S1

InChIKey=PHDLAANJDCSOQS-ZLUOBGJFSA-N

C10H12ClN5O2S

301.75

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Thionucleosides

Not available

Thionucleosides

6-aminopurines Aminopyrimidines and derivatives 2-halopyrimidines N-substituted imidazoles Imidolactams Aryl chlorides Thiolanes Heteroaromatic compounds Secondary alcohols Dialkylthioethers Azacyclic compounds Primary amines Primary alcohols Organochlorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine thionucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Aryl chloride - N-substituted imidazole - Aryl halide - Imidolactam - Pyrimidine - Heteroaromatic compound - Imidazole - Thiolane - Azole - Secondary alcohol - Azacycle - Organoheterocyclic compound - Dialkylthioether - Thioether - Primary alcohol - Primary amine - Organic oxygen compound - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - 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