CCC1=NC(=NN1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(NCCN1CCOCC1)N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey=NOYRFHBSCWDJGK-CKXMCULTSA-N

C33H40N10O4

640.749

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

Not available

Not available

5'-deoxyribonucleosides

Diphenylmethanes 6-alkylaminopurines Glycosylamines Aminopyrimidines and derivatives N-substituted imidazoles Morpholines Imidolactams Triazoles Oxolanes Heteroaromatic compounds Trialkylamines Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Dialkyl ethers Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

5'-deoxyribonucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Monocyclic benzene moiety - Morpholine - N-substituted imidazole - Oxazinane - Pyrimidine - Imidolactam - Benzenoid - Azole - Oxolane - 1,2,4-triazole - Heteroaromatic compound - Imidazole - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-diol - Oxacycle - Ether - Dialkyl ether - Organoheterocyclic compound - Azacycle - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Organonitrogen compound - Organic nitrogen compound - Alcohol - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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