CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(NCCC1=CC=C(CCC(=O)NCCNC(=O)CC3=CC=C(N)C=C3)C=C1)N=C2N

InChIKey=YACZPSXUHHLMLM-CKXMCULTSA-N

C33H42N10O6

674.763

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

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

Aromatic heteropolycyclic compounds

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