[Na+].NC1=NC=NC2=C1N=C(Cl)N2[C@@H]1O[C@@H]2COP([O-])(=S)O[C@H]2[C@H]1O

InChIKey=ZEIVWYWIXCJSBP-QKAIHBBZSA-M

C10H10ClN5NaO5PS

401.69

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 Aryl chlorides Imidolactams Monosaccharides N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Organic metal halides Organic sodium salts Organic zwitterions Primary amines Hydrocarbon derivatives Organic oxides Organochlorides

Aromatic heteropolycyclic compounds

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