COC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COCC2=CC=CC=C2)[C@@H](O[C@H]2O[C@H](COCC3=CC=CC=C3)[C@@H](O)[C@H](O)[C@H]2OCC2=CC=CC=C2)[C@H]1O

InChIKey=KTCZAKFKZQFFGJ-AMLRBRGISA-N

C38H42N4O10

714.772

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines O-glycosyl compounds Hypoxanthines Benzylethers Alkyl aryl ethers Pyrimidines and pyrimidine derivatives Oxanes N-substituted imidazoles Monosaccharides Oxolanes Heteroaromatic compounds Secondary alcohols Acetals Oxacyclic compounds Azacyclic compounds Dialkyl ethers Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - O-glycosyl compound - Hypoxanthine - Benzylether - Purine - Imidazopyrimidine - Alkyl aryl ether - Monosaccharide - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Pyrimidine - Oxane - Azole - Imidazole - Oxolane - Heteroaromatic compound - Secondary alcohol - Acetal - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - 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