NC1=NC=NC2=C1N=CN2C1OC(CO)C2OP(O)(=S)OC12

InChIKey=OMSUUENXGWGOLC-UHFFFAOYSA-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 Primary aromatic amines N-substituted imidazoles Monosaccharides Imidolactams Oxolanes Heteroaromatic compounds Dioxaphospholanes Oxacyclic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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