CNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NCCC1=CC(=C(O)C(=C1)C(C)(C)C)C(C)(C)C

InChIKey=TWCLKOCYGIQUJU-UGCAPWQASA-N

C27H38N6O5

526.638

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-alkylaminopurines Glycosylamines Phenylpropanes Secondary alkylarylamines Aminopyrimidines and derivatives Phenols Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary carboxylic acid amides 1,2-diols Secondary alcohols Amino acids and derivatives Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteropolycyclic compounds

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