CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(N=C2NC(=O)NC1=CC=C(OC)C=C1)C#CC1=CC=CC=C1

InChIKey=LQABHXVNHYSTHF-NBCVKUGOSA-N

C28H27N7O6

557.567

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines N-phenylureas Purines and purine derivatives Methoxyanilines Phenoxy compounds Anisoles Methoxybenzenes Alkyl aryl ethers Pyrimidines and pyrimidine derivatives Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols Ureas 1,2-diols Oxacyclic compounds Azacyclic compounds Carbonyl compounds Organonitrogen compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - N-phenylurea - Imidazopyrimidine - Purine - Methoxyaniline - Anisole - Phenoxy compound - Phenol ether - Methoxybenzene - Alkyl aryl ether - Imidolactam - Benzenoid - Monocyclic benzene moiety - N-substituted imidazole - Pyrimidine - Imidazole - Azole - Oxolane - Heteroaromatic compound - 1,2-diol - Secondary carboxylic acid amide - Carboxamide group - Secondary alcohol - Urea - Oxacycle - Organoheterocyclic compound - Ether - Carboxylic acid derivative - Azacycle - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Alcohol - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen 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