[Na+].NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]2COP([O-])(=S)O[C@H]2[C@H]1O

InChIKey=YTUKZYORDGLGPR-NVGWRVNNSA-M

C10H11N5NaO5PS

367.25

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 Aminopyrimidines and derivatives Thiophosphoric acid esters Imidolactams Monosaccharides N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Organic zwitterions Hydrocarbon derivatives Primary amines Organic sodium salts Organic oxides

Aromatic heteropolycyclic compounds

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