NC1=NC(Cl)=NC2=C1N=CN2[C@@H]1O[C@@H]2COP(O)(=S)O[C@H]2[C@H]1O

InChIKey=PMTFGHJSNPKVBG-QVRNUERCSA-N

C10H11ClN5O5PS

379.71

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3',5'-cyclic purine nucleoside phosphorothioates

Not available

3',5'-cyclic purine nucleoside phosphorothioates

Glycosylamines 6-aminopurines Thiophosphate diesters 2-halopyrimidines Aminopyrimidines and derivatives N-substituted imidazoles Monosaccharides Imidolactams Aryl chlorides Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Organochlorides Hydrocarbon derivatives Primary amines

Aromatic heteropolycyclic compounds

3',5'-cyclic purine nucleoside phosphorothioate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Thiophosphate diester - Aryl chloride - Aryl halide - Monosaccharide - N-substituted imidazole - Thiophosphoric acid ester - Pyrimidine - Imidolactam - Organic thiophosphoric acid or derivatives - Azole - Oxolane - Heteroaromatic compound - Imidazole - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Alcohol - Organohalogen compound - Hydrocarbon derivative - Organooxygen compound - Primary amine - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Organochloride - Amine - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as 3',5'-cyclic purine nucleoside phosphorothioates. These are 3',5'-cyclic purine nucleoside phosphate analogues, where a phosphate oxygen has been exchanged for sulphur generating a chiral phosphorothioate. In 3',5'-cyclic nucleoside phosphorothioate, the oxygen atoms at the 3'- and 5'-positions of the ribose are part of the phosphorothioate group.

Not available