CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(N=C2N)C#CCN1CCN(C)CC1

InChIKey=WKMDMQGIZQDCQF-KSVNGYGVSA-N

C20H28N8O4

444.496

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-aminopurines N-methylpiperazines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Trialkylamines Secondary carboxylic acid amides Secondary alcohols 1,2-diols Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Primary amines Carbonyl compounds

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-methylpiperazine - N-alkylpiperazine - 1,4-diazinane - N-substituted imidazole - Piperazine - Pyrimidine - Imidolactam - Oxolane - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carboxamide group - 1,2-diol - Azacycle - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Amine - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Alcohol - Primary amine - 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