CC(C(NC1=NC=NC2=C1N=CN2C1OC(CO)C(O)C1O)C(O)=O)C(O)=O

InChIKey=HWVUUTNORPSCNF-UHFFFAOYSA-N

C15H19N5O8

397.344

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-alkylaminopurines Glycosylamines Pentoses Alpha amino acids and derivatives Secondary alkylarylamines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Dicarboxylic acids and derivatives Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Amino acids Oxacyclic compounds Carboxylic acids Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds Primary alcohols

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Alpha-amino acid or derivatives - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Dicarboxylic acid or derivatives - Monosaccharide - N-substituted imidazole - Pyrimidine - Imidolactam - Tetrahydrofuran - Heteroaromatic compound - Azole - Imidazole - Amino acid or derivatives - Secondary alcohol - Amino acid - Azacycle - Oxacycle - Secondary amine - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Amine - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Alcohol - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - 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