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

InChIKey=OMSUUENXGWGOLC-IINQOKOESA-N

C10H12N5O5PS

345.27

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 Thiophosphate diesters Aminopyrimidines and derivatives N-substituted imidazoles Monosaccharides Imidolactams Oxolanes Heteroaromatic compounds Dioxaphospholanes Oxacyclic compounds Azacyclic compounds Primary amines Primary alcohols Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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