NC1=NC(=O)N(C=C1)[C@@H]1CS[C@H](CO)O1.OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)C1C=CC(=O)NC1=O

InChIKey=KWGKMKMJDJFJCS-BCHHXAQYSA-N

C18H24N4O9S

472.47

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3'-thia pyrimidine nucleosides

Not available

3'-thia pyrimidine nucleosides

C-glycosyl compounds Pentoses Aminopyrimidines and derivatives Pyrimidones Hydropyridines Hydropyrimidines Imidolactams Dicarboximides Heteroaromatic compounds Oxolanes Oxathiolanes Monothioacetals N-unsubstituted carboxylic acid imides Secondary alcohols 1,2-diols Azacyclic compounds Dialkyl ethers Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Primary amines Carbonyl compounds Organic oxides

Not available

3'-thia pyrimidine nucleoside - C-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Monosaccharide - Hydropyrimidine - Pyrimidine - Imidolactam - Hydropyridine - Carboxylic acid imide - Oxathiolane - Monothioacetal - Carboxylic acid imide, n-unsubstituted - Heteroaromatic compound - Oxolane - Dicarboximide - Secondary alcohol - 1,2-diol - Carboxylic acid derivative - Dialkyl ether - Oxacycle - Ether - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Amine - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as 3'-thia pyrimidine nucleosides. These are nucleoside analogues with a structure that consists of a pyrimidine base, which is N-substituted at the 1-position with a 3'-thia derivative (1,3-oxazolidine) of the ribose moiety that is characteristic of nucleosides.

Not available