NC1=NC=NC2=C1N=C(NN=CC1=CC=C(O1)[N+]([O-])=O)N2C1OC(CO)C(O)C1O

InChIKey=UGCCNZSJRBTPTF-UHFFFAOYSA-N

C15H16N8O7

420.342

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-aminopurines Pentoses Nitroaromatic compounds Nitrofurans Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Oxacyclic compounds Hydrazones Organic oxoazanium compounds Primary alcohols Hydrocarbon derivatives Organic zwitterions Organic salts Primary amines Organic oxides

Aromatic heteropolycyclic compounds

Purine nucleoside - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Pentose monosaccharide - Purine - Imidazopyrimidine - Nitroaromatic compound - 2-nitrofuran - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Monosaccharide - Imidazole - Azole - Furan - Oxolane - Heteroaromatic compound - Secondary alcohol - Organic nitro compound - C-nitro compound - Hydrazone - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxoazanium - Organoheterocyclic compound - Azacycle - Oxacycle - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Alcohol - 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