OC[C@@H]1CN(C[C@H]1CC1=CC=CC=C1)C1=NC2=C(N=CN2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(NCC(C2=CC=CC=C2)C2=CC=CC=C2)=N1

InChIKey=SOFSSTCNLYDINS-YQULSPBESA-N

C36H40N6O5

636.753

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 Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives 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 - Imidolactam - Benzenoid - Monosaccharide - N-substituted imidazole - Pyrimidine - Imidazole - Pyrrolidine - Azole - Heteroaromatic compound - Oxolane - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Primary alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Amine - 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