CCC1=NC(=NO1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(NCCN1CCCCC1)N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey=MWAFNAFZJUAOKP-KCIBBDPESA-N

C34H41N9O4

639.761

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

Not available

Not available

5'-deoxyribonucleosides

Diphenylmethanes Glycosylamines 6-alkylaminopurines Aminopyrimidines and derivatives Piperidines N-substituted imidazoles Imidolactams Oxolanes 1,2,4-oxadiazoles Heteroaromatic compounds Trialkylamines Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

5'-deoxyribonucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Piperidine - Pyrimidine - Imidolactam - Benzenoid - Oxolane - Oxadiazole - Imidazole - Heteroaromatic compound - Azole - 1,2,4-oxadiazole - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Amine - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

Not available