CC1=CC=CC=C1CN1C=C(CCNC2=NC=NC3=C2N=CN3C2OC(C(O)C2O)C(=O)NC2CC2)C2=CC=CC=C12

InChIKey=WBPQPPNWGRXBKK-UHFFFAOYSA-N

C31H33N7O4

567.65

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-alkylaminopurines Glycosylamines 3-alkylindoles N-alkylindoles Toluenes Secondary alkylarylamines Aminopyrimidines and derivatives Substituted pyrroles Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary carboxylic acid amides 1,2-diols Amino acids and derivatives Secondary alcohols Oxacyclic compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - N-alkylindole - 3-alkylindole - Imidazopyrimidine - Indole - Indole or derivatives - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Toluene - Substituted pyrrole - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Imidolactam - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Pyrrole - Oxolane - Secondary carboxylic acid amide - 1,2-diol - Secondary alcohol - Amino acid or derivatives - Carboxamide group - Azacycle - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Secondary amine - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Amine - Organic oxide - 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