NC1=NC(=O)C2=C(N1)N(C=N2)[C@@H]1O[C@H](CO)[C@H]2OP(O)(=S)O[C@@H]12

InChIKey=QZEROIIFJLCOOE-QVRNUERCSA-N

C10H12N5O6PS

361.27

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-oxopurines Hypoxanthines Thiophosphate diesters Pyrimidones Aminopyrimidines and derivatives Monosaccharides N-substituted imidazoles Vinylogous amides Dioxaphospholanes Heteroaromatic compounds Oxolanes Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Primary amines Organic oxides

Aromatic heteropolycyclic compounds

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