OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1)N1CC[C@@H](C1)NC(=O)N[C@H]1CCNC1

InChIKey=YYILZUZHLPMBRB-JQOMMHAYSA-N

C33H41N9O5

643.749

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Diphenylmethanes 6-alkylaminopurines Glycosylamines Pentoses Dialkylarylamines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Pyrrolidines Secondary alcohols Ureas Oxacyclic compounds Dialkylamines Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary alcohols

Aromatic heteropolycyclic compounds

Purine nucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Imidolactam - Pyrimidine - Benzenoid - Azole - Oxolane - Pyrrolidine - Imidazole - Heteroaromatic compound - Urea - Secondary alcohol - Organoheterocyclic compound - Azacycle - Secondary amine - Secondary aliphatic amine - Oxacycle - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Carbonyl group - Organic nitrogen compound - Amine - Organonitrogen compound - Organooxygen compound - 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