COC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(CNC1CCC(CC1)OC)N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey=ZMTXAQLFGQGDRR-OWAPMMQCSA-N

C33H42N6O5

602.736

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Diphenylmethanes 6-alkylaminopurines Glycosylamines Pentoses Secondary alkylarylamines Aminopyrimidines and derivatives Aralkylamines Cyclohexylamines N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Dialkylamines Dialkyl ethers Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine nucleoside - Diphenylmethane - N-glycosyl compound - Glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Aralkylamine - Secondary aliphatic/aromatic amine - Cyclohexylamine - Pyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Imidolactam - Benzenoid - Azole - Oxolane - Heteroaromatic compound - Imidazole - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkyl ether - Secondary aliphatic amine - Secondary amine - Ether - Organic oxygen compound - Alcohol - Amine - Hydrocarbon derivative - Organic nitrogen compound - 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