CC(=O)C1=CC2=C(C=C1)C1=C(C2)C=C(NC2=NC3=C(NC(N)=NC3=O)N2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=C1

InChIKey=SGZXPMIODCKRFV-ZDXOVATRSA-N

C25H24N6O6

504.503

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Fluorenes Glycosylamines Pentoses Hypoxanthines 6-oxopurines Acetophenones Aryl alkyl ketones Pyrimidones Aminopyrimidines and derivatives N-substituted imidazoles Aminoimidazoles Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Secondary amines Oxacyclic compounds Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine nucleoside - Fluorene - N-glycosyl compound - Glycosyl compound - Purinone - Pentose monosaccharide - Hypoxanthine - 6-oxopurine - Purine - Imidazopyrimidine - Acetophenone - Aryl alkyl ketone - Aryl ketone - Pyrimidone - Aminopyrimidine - Benzenoid - Pyrimidine - N-substituted imidazole - Monosaccharide - Aminoimidazole - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Imidazole - Azole - Secondary alcohol - Ketone - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen 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