NC1=NC(=O)N(C=C1)[C@@H]1CS[C@H](CO)O1.NC1=NC(=O)C2=C(N1)N(C=N2)[C@@H]1C[C@H](CO)[C@H]1CO

InChIKey=ZGOSUNWQZQNCAS-AXBRUAEOSA-N

C19H26N8O6S

494.53

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3'-thia pyrimidine nucleosides

Not available

3'-thia pyrimidine nucleosides

6-oxopurines Hypoxanthines Pyrimidones Aminopyrimidines and derivatives Hydropyrimidines Imidolactams N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxathiolanes Monothioacetals Azacyclic compounds Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Primary amines Organic oxides

Not available

3'-thia pyrimidine nucleoside - 6-oxopurine - Hypoxanthine - Purinone - Purine - Imidazopyrimidine - Aminopyrimidine - Pyrimidone - N-substituted imidazole - Hydropyrimidine - Pyrimidine - Imidolactam - Vinylogous amide - Imidazole - Heteroaromatic compound - Monothioacetal - Azole - Oxathiolane - Oxacycle - Azacycle - Organoheterocyclic compound - Primary amine - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Organonitrogen compound - Organooxygen compound - 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