[Na+].NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@H]2OP([O-])(=S)O[C@@H]12

InChIKey=PYTONXYLIVXPKO-NVGWRVNNSA-M

C10H11N5NaO5PS

367.25

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

2',3'-cyclic purine nucleoside phosphorothioates

Not available

2',3'-cyclic purine nucleoside phosphorothioates

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

Aromatic heteropolycyclic compounds

2',3'-cyclic purine nucleoside phosphorothioate - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Imidolactam - Organic thiophosphoric acid or derivatives - Pyrimidine - Monosaccharide - N-substituted imidazole - Thiophosphoric acid ester - Heteroaromatic compound - Azole - 1,3_dioxaphospholane - Imidazole - Oxolane - Oxacycle - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Organic oxide - Organooxygen compound - Organonitrogen compound - Primary alcohol - Primary amine - Alcohol - Organic nitrogen compound - Organic zwitterion - Organic oxygen compound - Organic salt - Organic sodium salt - Amine - Hydrocarbon derivative - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as 2',3'-cyclic purine nucleoside phosphorothioates. These are 2',3'-cyclic purine nucleoside phosphate analogues, where a phosphate oxygen has been exchanged for sulphur generating a chiral phosphorothioate. In 2',3'-cyclic nucleoside phosphorothioate, the oxygen atoms at the 2'- and 3'-positions of the ribose are part of the phosphorothioate group.

Not available