CCC1=NC(=NO1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(NC(CO)CC1=CC=CC=C1)N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey=NLFNOIKNUZWBEM-ZXNFFLIHSA-N

C36H38N8O5

662.751

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

Not available

Not available

5'-deoxyribonucleosides

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

Aromatic heteropolycyclic compounds

5'-deoxyribonucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Amphetamine or derivatives - Imidazopyrimidine - Purine - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Pyrimidine - Benzenoid - Oxolane - Oxadiazole - Azole - 1,2,4-oxadiazole - Heteroaromatic compound - Imidazole - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Primary alcohol - Alcohol - Organic oxygen compound - Organooxygen 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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