CNC1=NC(=NC2=C1N=CN2C1O[C@H](CO)[C@@H](O)[C@H]1O)N1C=C(C=N1)C1=CC=C(OC)C=C1

InChIKey=PBPQOBBHDIVSFT-FIALEDGQSA-N

C21H23N7O5

453.459

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-alkylaminopurines Glycosylamines Phenylpyrazoles Pentoses Anisoles Methoxybenzenes Phenoxy compounds Secondary alkylarylamines Aminopyrimidines and derivatives Alkyl aryl ethers N-substituted imidazoles Imidolactams Heteroaromatic compounds Oxolanes Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols

Aromatic heteropolycyclic compounds

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