[H][C@]1(CO)O[C@@]([H])(N2C=NC3=C2NC(=N)N=C3O)[C@]2([H])O[P@@](O)(=S)O[C@]12[H]

InChIKey=QZEROIIFJLCOOE-FHIGPPGSSA-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

Purines and purine derivatives Thiophosphate diesters Hydroxypyrimidines N-substituted imidazoles Monosaccharides Tetrahydrofurans Heteroaromatic compounds Dioxaphospholanes Oxacyclic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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