NC1=NC=NC2=C1N=CN2C1OC2COP(O)(=S)O[C@@H]2[C@@H]1O

InChIKey=SMPNJFHAPJOHPP-PKZJYKHDSA-N

C10H12N5O5PS

345.27

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 Aminopyrimidines and derivatives N-substituted imidazoles Monosaccharides Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary amines Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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