NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O.OC([C@H]1O[C@H]([C@H](O)[C@@]1(O)P(O)(O)=O)N1C=CC(=O)NC1=O)P(O)(O)=O

InChIKey=SDUVGHXIFKCQET-MTYNSZFXSA-N

C19H27N7O16P2

671.406

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-aminopurines Aminopyrimidines and derivatives Pyrimidones Hydropyrimidines Imidolactams Monosaccharides N-substituted imidazoles Organic phosphonic acids Vinylogous amides Heteroaromatic compounds Oxolanes Lactams Ureas Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organophosphorus compounds Primary alcohols Primary amines

Not available

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - N-substituted imidazole - Imidolactam - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Organophosphonic acid - Organophosphonic acid derivative - Oxolane - Vinylogous amide - Secondary alcohol - Urea - Lactam - Oxacycle - Organoheterocyclic compound - Azacycle - Organooxygen compound - Organic oxygen compound - Amine - Alcohol - Hydrocarbon derivative - Organophosphorus compound - Organic nitrogen compound - Primary alcohol - Primary amine - Organic oxide - Organonitrogen 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