CO[C@@H]1[C@H](OP(O)(=S)OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@](C)(O)[C@@H]2O)[C@@H](CO)O[C@H]1N1C=NC2=C1N=CN=C2N

InChIKey=DDAFRSBMIJFHNT-PWPXIXHISA-N

C21H29N8O10PS

616.54

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrimidine nucleosides

Not available

Not available

Pyrimidine nucleosides

Glycosylamines 6-aminopurines Thiophosphate diesters Aminopyrimidines and derivatives Pyrimidones Hydropyrimidines Imidolactams Monosaccharides N-substituted imidazoles Tertiary alcohols Heteroaromatic compounds Oxolanes Secondary alcohols 1,2-diols Azacyclic compounds Dialkyl ethers Oxacyclic compounds Hydrocarbon derivatives Primary amines Organic oxides Primary alcohols

Aromatic heteropolycyclic compounds

Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Thiophosphate diester - Organic thiophosphoric acid or derivatives - Imidolactam - Hydropyrimidine - Monosaccharide - N-substituted imidazole - Pyrimidine - Thiophosphoric acid ester - Azole - Tertiary alcohol - Imidazole - Oxolane - Heteroaromatic compound - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organooxygen compound - Amine - Primary alcohol - Primary amine - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.

Not available