CCCCN(CCCC)CCN(C)C(=O)NCC1=NC2=C(N=CN2[C@@H]2O[C@@H]([C@@H](O)[C@H]2O)C(=O)NCC)C(NCC(C2=CC=CC=C2)C2=CC=CC=C2)=N1

InChIKey=DXWDGEOCHDKTKX-VIBCZQBBSA-N

C39H55N9O5

729.927

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 Ureas Trialkylamines Secondary carboxylic acid amides Secondary alcohols 1,2-diols Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteropolycyclic compounds

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