COCC1=C2[C@H](CCN2C=C1)NC1=NC(=O)C2=C(N1)N(C=N2)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChIKey=LNKJGCQBAQRCQT-MBRXSIFGSA-N

C19H24N6O6

432.437

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines Pentoses Hypoxanthines 6-oxopurines Pyrrolizines Secondary alkylarylamines Pyrimidones Aminopyrimidines and derivatives Substituted pyrroles N-substituted imidazoles Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Dialkyl ethers Azacyclic compounds Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine nucleoside - N-glycosyl compound - Glycosyl compound - Purinone - Pentose monosaccharide - Hypoxanthine - 6-oxopurine - Purine - Imidazopyrimidine - Pyrrolizine - Secondary aliphatic/aromatic amine - Pyrimidone - Aminopyrimidine - Substituted pyrrole - Pyrimidine - N-substituted imidazole - Monosaccharide - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Pyrrole - Imidazole - Azole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - 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