NC1=NC(NC(=O)C=CC2=CC=CC=C2)=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChIKey=DDCUXRNACUVAKE-XKLVTHTNSA-N

C19H20N6O5

412.406

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Cinnamic acid amides Glycosylamines 6-aminopurines Pentoses N-arylamides Styrenes Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols Amino acids and derivatives Secondary carboxylic acid amides Oxacyclic compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Primary amines Primary alcohols

Aromatic heteropolycyclic compounds

Purine nucleoside - Cinnamic acid amide - Cinnamic acid or derivatives - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - N-arylamide - Styrene - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Imidolactam - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Imidazole - Oxolane - Amino acid or derivatives - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Primary alcohol - Hydrocarbon derivative - Alcohol - Amine - Carbonyl group - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Primary 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