CCNC(=O)[C@H]1OC([C@H](O)[C@@H]1O)N1C=NC2=C1N=C[N+](CC1=CC=C(C=C1)[N+]([O-])=O)=C2N

InChIKey=GSAKMKLTYAVZPB-FRLFKWGPSA-O

C19H22N7O6

444.427

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-aminopurines Nitrobenzenes Nitroaromatic compounds Aminopyrimidines and derivatives N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols 1,2-diols Amino acids and derivatives Oxacyclic compounds Organic oxoazanium compounds Azacyclic compounds Primary amines Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic salts Organic cations

Aromatic heteropolycyclic compounds

Purine nucleoside - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Purine - Imidazopyrimidine - Nitrobenzene - Nitroaromatic compound - Aminopyrimidine - Benzenoid - Monocyclic benzene moiety - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Azole - Oxolane - Imidazole - 1,2-diol - Amino acid or derivatives - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Azacycle - Organic oxoazanium - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Carbonyl group - Organic salt - Hydrocarbon derivative - Organic oxide - Amine - Alcohol - Organic cation - 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