CC1=CC=C(C=C1)S(=O)(=O)O[C@@H]1[C@@H](CO)O[C@](C#N)([C@@H]1O)N1C=C(C)C(=O)NC1=O

InChIKey=NCICUAKWYVQIQD-ATNYBXOESA-N

C18H19N3O8S

437.42

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrimidine nucleosides

Not available

Not available

Pyrimidine nucleosides

p-Methylbenzenesulfonates Benzenesulfonate esters C-glycosyl compounds Tosyl compounds Arylsulfonic acids and derivatives Benzenesulfonyl compounds Pyrimidones Hydropyrimidines Monosaccharides Organosulfonic acid esters Vinylogous amides Sulfonyls Heteroaromatic compounds Oxolanes Lactams Ureas Secondary alcohols Azacyclic compounds Nitriles Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Organic oxides

Aromatic heteromonocyclic compounds

Pyrimidine nucleoside - C-glycosyl compound - Glycosyl compound - Benzenesulfonate ester - P-methylbenzenesulfonate - Benzenesulfonate - Tosyl compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Pyrimidone - Toluene - Monocyclic benzene moiety - Pyrimidine - Hydropyrimidine - Organosulfonic acid ester - Monosaccharide - Benzenoid - Heteroaromatic compound - Sulfonyl - Organic sulfonic acid or derivatives - Oxolane - Organosulfonic acid or derivatives - Vinylogous amide - Secondary alcohol - Urea - Lactam - Oxacycle - Azacycle - Carbonitrile - Nitrile - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Cyanide - Primary alcohol - Aromatic heteromonocyclic 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