CCN1N=NC(=N1)[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=CCYUSUQOSHABQD-OVDFTCDZSA-N

C32H39N11O4

641.737

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

Not available

Not available

5'-deoxyribonucleosides

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

Aromatic heteropolycyclic compounds

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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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