CC(C)N1N=NC(=N1)[C@H]1O[C@H]([C@H](OC=O)[C@@H]1O)N1C=NC2=C1N=C(NCCC1=CN(C)C=N1)N=C2NC1CCCC1

InChIKey=NBUJLDCXXBDKSG-ZBNTXBBCSA-N

C25H34N12O4

566.627

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

Not available

Not available

5'-deoxyribonucleosides

6-alkylaminopurines Glycosylamines Secondary alkylarylamines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Tetrazoles Oxolanes Heteroaromatic compounds Secondary alcohols Amino acids and derivatives Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

5'-deoxyribonucleoside - 6-alkylaminopurine - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Pyrimidine - Imidolactam - N-substituted imidazole - Imidazole - Tetrazole - Oxolane - Azole - Heteroaromatic compound - Amino acid or derivatives - Carboxylic acid ester - Secondary alcohol - Secondary amine - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Hydrocarbon derivative - Alcohol - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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