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

InChIKey=DDCUXRNACUVAKE-HGBQRMJASA-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 Styrenes N-arylamides Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds 1,2-diols Secondary alcohols Secondary carboxylic acid amides Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary amines Primary alcohols

Aromatic heteropolycyclic compounds

Purine nucleoside - Cinnamic acid or derivatives - Cinnamic acid amide - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - 6-aminopurine - Imidazopyrimidine - Purine - N-arylamide - Styrene - Aminopyrimidine - Benzenoid - Pyrimidine - Monosaccharide - Monocyclic benzene moiety - Imidolactam - N-substituted imidazole - Oxolane - Imidazole - Azole - Heteroaromatic compound - 1,2-diol - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Amine - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Primary amine - Primary alcohol - 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