CC1=CN([C@@H]2O[C@H](CO)C=C2)C(=O)NC1=O.NC1=NC(=O)N(C=C1F)[C@@H]1CS[C@H](CO)O1

InChIKey=SZXMCMJQLJDFNX-OGYPRSBESA-N

C18H22FN5O7S

471.46

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3'-thia pyrimidine nucleosides

Not available

3'-thia pyrimidine nucleosides

Aminopyrimidines and derivatives Pyrimidones Halopyrimidines Aryl fluorides Hydropyrimidines Imidolactams Vinylogous amides Dihydrofurans Heteroaromatic compounds Oxathiolanes Monothioacetals Lactams Ureas Azacyclic compounds Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Primary amines Organic oxides Organofluorides Organopnictogen compounds

Not available

3'-thia pyrimidine nucleoside - Aminopyrimidine - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - Imidolactam - Pyrimidine - Dihydrofuran - Heteroaromatic compound - Monothioacetal - Vinylogous amide - Oxathiolane - Lactam - Urea - Oxacycle - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Primary amine - Primary alcohol - 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