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@@H]1O)N1C=NC2=C1NC=NC[C@H]2O

InChIKey=SIOJWKUGYWBRIQ-YDGRPDDMSA-N

C21H29N9O9

551.517

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-aminopurines Imidazodiazepines 1,3-diazepines Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Monosaccharides Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Formamidines Carboxamidines Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Primary amines

Not available

Purine nucleoside - N-glycosyl compound - Glycosyl compound - Imidazodiazepine - Imidazo-meta-diazepine - 6-aminopurine - Purine - Imidazopyrimidine - Meta-diazepine - Aminopyrimidine - Imidolactam - Monosaccharide - N-substituted imidazole - Pyrimidine - Oxolane - Imidazole - Azole - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Formamidine - Amidine - Oxacycle - Carboxylic acid amidine - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Alcohol - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - 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