CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey=LEEIBBJHEJYQOJ-IMIIHFCZSA-N

C26H28N6O4

488.548

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Diphenylmethanes 6-alkylaminopurines Glycosylamines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Amines Organic oxides Carbonyl compounds

Aromatic heteropolycyclic compounds

Purine nucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - N-substituted imidazole - Monocyclic benzene moiety - Pyrimidine - Imidolactam - Benzenoid - Heteroaromatic compound - Imidazole - Oxolane - Azole - 1,2-diol - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alcohol - Amine - Organooxygen 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