CCCC(=O)NC1=NC(=O)C2=C(N1)N([C@@H]1O[C@H](COC(=O)CCC)[C@@H](OC(=O)CCC)[C@H]1OC(=O)CCC)C(=O)N2CC=C

InChIKey=VVPYDKGPQFCUQN-ZHKMAXBCSA-N

C29H41N5O10

619.672

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-oxopurines Hypoxanthines Tricarboxylic acids and derivatives N-arylamides Fatty acid esters Pyrimidones Fatty amides Monosaccharides N-substituted imidazoles Oxolanes Heteroaromatic compounds Vinylogous amides Secondary carboxylic acid amides Ureas Carboxylic acid esters Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Tricarboxylic acid or derivatives - N-arylamide - Fatty acid ester - Pyrimidone - Fatty amide - Monosaccharide - N-substituted imidazole - Fatty acyl - Pyrimidine - Oxolane - Vinylogous amide - Azole - Heteroaromatic compound - Imidazole - Urea - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Oxacycle - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Organic oxygen 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