NC1=NC(=O)N(C=C1F)[C@@H]1CS[C@H](CO)O1.NC1=NC=NC2=C1N=CN2CCOCP(O)(O)=O

InChIKey=LEAINGIBMJPQIB-RIHPBJNCSA-N

C16H22FN8O7PS

520.43

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3'-thia pyrimidine nucleosides

Not available

3'-thia pyrimidine nucleosides

6-aminopurines Pyrimidones Aminopyrimidines and derivatives Halopyrimidines Primary aromatic amines Aryl fluorides Hydropyrimidines Imidolactams N-substituted imidazoles Oxathiolanes Heteroaromatic compounds Monothioacetals Organic phosphonic acids Oxacyclic compounds Azacyclic compounds Organophosphorus compounds Hydrocarbon derivatives Primary alcohols Organopnictogen compounds Organofluorides Organic oxides

Not available

3'-thia pyrimidine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - N-substituted imidazole - Primary aromatic amine - Pyrimidine - Imidolactam - Oxathiolane - Heteroaromatic compound - Azole - Imidazole - Monothioacetal - Organophosphonic acid derivative - Organophosphonic acid - Azacycle - Organoheterocyclic compound - Oxacycle - Primary amine - Organohalogen compound - Organic oxygen compound - Organofluoride - Organic oxide - Organonitrogen compound - Amine - Organopnictogen compound - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organophosphorus compound - Primary alcohol - Alcohol - Aromatic heteropolycyclic 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