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

InChIKey=KKZXMAPICHTJLL-TVYQEYQBSA-N

C31H37N7O5

587.681

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Diphenylmethanes 6-alkylaminopurines Glycosylamines Secondary alkylarylamines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Cyclopentanols Tetrahydrofurans Heteroaromatic compounds Secondary carboxylic acid amides Amino acids and derivatives Cyclic alcohols and derivatives Oxacyclic compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds

Aromatic heteropolycyclic compounds

Purine nucleoside - Diphenylmethane - N-glycosyl compound - Glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - N-substituted imidazole - Monocyclic benzene moiety - Cyclopentanol - Imidolactam - Benzenoid - Pyrimidine - Imidazole - Azole - Heteroaromatic compound - Cyclic alcohol - Tetrahydrofuran - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Secondary amine - Alcohol - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Organopnictogen 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