CCOC1=CC=CC(=C1)C1=CC=C(CNC2=NC3=C(N=CN=C3N)N2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=C1

InChIKey=AONSBDSWBNUHDS-UMCMBGNQSA-N

C25H28N6O5

492.536

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Biphenyls and derivatives Glycosylamines 6-aminopurines Pentoses Phenoxy compounds Phenol ethers Benzylamines Secondary alkylarylamines Alkyl aryl ethers Aminopyrimidines and derivatives Aminoimidazoles N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives Primary amines

Aromatic heteropolycyclic compounds

Purine nucleoside - Biphenyl - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - 6-aminopurine - Imidazopyrimidine - Purine - Benzylamine - Phenoxy compound - Phenol ether - Aminopyrimidine - Alkyl aryl ether - Secondary aliphatic/aromatic amine - Pyrimidine - N-substituted imidazole - Benzenoid - Monosaccharide - Imidolactam - Aminoimidazole - Monocyclic benzene moiety - Heteroaromatic compound - Azole - Imidazole - Oxolane - 1,2-diol - Secondary alcohol - Oxacycle - Secondary amine - Ether - Organoheterocyclic compound - Azacycle - Organooxygen compound - Alcohol - Organic nitrogen compound - Primary amine - Hydrocarbon derivative - Amine - Primary alcohol - Organic oxygen compound - Organonitrogen compound - 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