CC1=CC=CC=C1NC(=O)CC1=CC=C(NC2=NC=NC3=C2N=CN3C2OC(CO)C(O)C2O)C=C1

InChIKey=GSNAEQKSRSPWCT-UHFFFAOYSA-N

C25H26N6O5

490.52

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-aminopurines Pentoses Phenylacetamides Anilides Aniline and substituted anilines N-arylamides Aminopyrimidines and derivatives Toluenes N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols Amino acids and derivatives Secondary carboxylic acid amides 1,2-diols Azacyclic compounds Oxacyclic compounds Secondary amines Primary alcohols Carbonyl compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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