COC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(CSC1=CC=CC=C1)N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey=IRZLKLDTTWGIDK-FANUBLADSA-N

C32H33N5O4S

583.71

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Diphenylmethanes 6-alkylaminopurines Glycosylamines Pentoses Thiophenol ethers Alkylarylthioethers Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds 1,2-diols Secondary alcohols Oxacyclic compounds Dialkyl ethers Azacyclic compounds Sulfenyl compounds Amines Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine nucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Purine - Imidazopyrimidine - Aryl thioether - Thiophenol ether - Aminopyrimidine - Alkylarylthioether - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Pyrimidine - Monosaccharide - Benzenoid - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - 1,2-diol - Thioether - Sulfenyl compound - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organooxygen compound - Organosulfur compound - Amine - 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