CCC(C)(C[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(N)N=C2OC)OP(O)(=O)C(C)(O)CC

InChIKey=FFMANFUVKVKUBE-SDLSHWKWSA-N

C19H32N5O8P

489.466

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

Not available

Not available

5'-deoxyribonucleosides

Glycosylamines Pentoses Hypoxanthines Alkyl aryl ethers Aminopyrimidines and derivatives Phosphonic acid esters N-substituted imidazoles Oxolanes Organic phosphonic acids Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Organophosphorus compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

5'-deoxyribonucleoside - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Hypoxanthine - Purine - Imidazopyrimidine - Alkyl aryl ether - Aminopyrimidine - Pyrimidine - Phosphonic acid ester - Monosaccharide - N-substituted imidazole - Heteroaromatic compound - Organophosphonic acid - Imidazole - Organophosphonic acid derivative - Oxolane - Azole - 1,2-diol - Secondary alcohol - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Primary amine - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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