[Na+].NC1=NC=NC2=C1N=C(N2[C@@H]1O[C@@H]2COP([O-])(=S)O[C@H]2[C@H]1O)C1=CC=CO1

InChIKey=OROIZAYENQXSPI-JYHPCZHOSA-M

C14H13N5NaO6PS

433.31

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 Furans Heteroaromatic compounds Oxolanes Secondary alcohols Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Primary amines Organic sodium salts Organic zwitterions

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 - Furan - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Organic alkali metal salt - Organic zwitterion - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Amine - Hydrocarbon derivative - Organic oxide - Alcohol - Organic nitrogen compound - Organic sodium salt - Primary amine - 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