NC1=NC2=C(N=CN2[C@H]2O[C@H](CO)[C@@H]3O[P@](O)(=S)O[C@H]23)C(=O)N1

InChIKey=QZEROIIFJLCOOE-PDBXSDAOSA-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 Aminopyrimidines and derivatives Pyrimidones Monosaccharides N-substituted imidazoles Vinylogous amides Tetrahydrofurans Dioxaphospholanes Heteroaromatic compounds Lactams Azacyclic compounds Oxacyclic compounds Primary amines Hydrocarbon derivatives Primary alcohols Organic oxides Organopnictogen compounds

Aromatic heteropolycyclic compounds

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