[O-][Cl](=O)(=O)=O.NC1=[N+](OCC2=CC=CC(=C2)C#N)C=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChIKey=HLIABDMTMXVDMQ-VHGNBCBTSA-N

C18H19ClN6O9

498.83

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-aminopurines Pentoses Benzonitriles Aminopyrimidines and derivatives N-substituted imidazoles Organic perchlorate salts Organic perchlorates Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Nitriles Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols Primary amines Organic oxides Organic zwitterions

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Benzonitrile - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - Organic perchlorate salt - N-substituted imidazole - Organic perchlorate - Benzenoid - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - 1,2-diol - Organic chlorate - Oxacycle - Azacycle - Nitrile - Carbonitrile - Organoheterocyclic compound - Amine - Organic salt - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Cyanide - Organooxygen compound - Organic oxygen compound - Organic zwitterion - Primary alcohol - Primary 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