NC(=O)C1=NN(C=N1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O.NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O

InChIKey=WETTWVKMBDYRIY-UXSIZVIPSA-N

C18H25N9O9

511.452

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Triazole ribonucleosides and ribonucleotides Glycosylamines 6-aminopurines 2-heteroaryl carboxamides Aminopyrimidines and derivatives Imidolactams Monosaccharides N-substituted imidazoles Triazoles Heteroaromatic compounds Oxolanes Primary carboxylic acid amides Secondary alcohols Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Primary amines Primary alcohols

Not available

Purine nucleoside - N-ribosyl-1,2,4-triazole - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - 2-heteroaryl carboxamide - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Pyrimidine - Imidolactam - 1,2,4-triazole - Triazole - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Primary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Amine - 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