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

InChIKey=REYFSXASQOSVEZ-JFLQNCKRSA-N

C19H30N5O12PS

583.51

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines O-glycosyl compounds 6-aminopurines Thiophosphate diesters Aminopyrimidines and derivatives Primary aromatic amines Imidolactams Oxanes Monosaccharides N-substituted imidazoles Heteroaromatic compounds Oxolanes Secondary alcohols Acetals Polyols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Organopnictogen compounds

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - O-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Thiophosphate diester - Organic thiophosphoric acid or derivatives - Imidolactam - Thiophosphoric acid ester - Pyrimidine - N-substituted imidazole - Monosaccharide - Primary aromatic amine - Oxane - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Azacycle - Oxacycle - Primary alcohol - Alcohol - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Primary amine - Amine - Organooxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

Not available