CN1C(=O)C2=C(N=C1\N=C\N(CC1=CC=CC=C1)CC1=CC=CC=C1)N(C=N2)[C@@H]1O[C@H](CO)[C@H]2OC(O[C@@H]12)C1=CC=CC=C1

InChIKey=KZANNILBXBDODB-BYKJXZBPSA-N

C33H32N6O5

592.656

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-oxopurines Hypoxanthines Pyrimidones Benzene and substituted derivatives N-substituted imidazoles Monosaccharides Vinylogous amides 1,3-dioxolanes Oxolanes Heteroaromatic compounds Lactams Propargyl-type 1,3-dipolar organic compounds Acetals Azacyclic compounds Oxacyclic compounds Formamidines Carboxamidines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Purine nucleoside - 6-oxopurine - Hypoxanthine - Purine - Imidazopyrimidine - Pyrimidone - Pyrimidine - Monocyclic benzene moiety - Benzenoid - N-substituted imidazole - Monosaccharide - Azole - Oxolane - Vinylogous amide - Meta-dioxolane - Imidazole - Heteroaromatic compound - Lactam - Formamidine - Acetal - Amidine - Carboxylic acid amidine - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Alcohol - Primary 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