[Na+].NC1=NC(=O)C2=C(N1)N(C=N2)[C@@H]1O[C@@H]2COP([O-])(=S)O[C@H]2[C@H]1O

InChIKey=ZGHLFNWZUBWIKY-QKAIHBBZSA-M

C10H11N5NaO6PS

383.25

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

Aromatic heteropolycyclic compounds

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