OC(=O)C1=CC=CC=C1O.NC1=NC(=O)N(C=C1)[C@@H]1CS[C@H](CO)O1

InChIKey=GFZSGYKUKMIFHP-UOERWJHTSA-N

C15H17N3O6S

367.38

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3'-thia pyrimidine nucleosides

Not available

3'-thia pyrimidine nucleosides

Salicylic acids Benzoic acids Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids Pyrimidones 1-hydroxy-4-unsubstituted benzenoids Aminopyrimidines and derivatives Hydropyrimidines Imidolactams Vinylogous acids Heteroaromatic compounds Oxathiolanes Monothioacetals Carboxylic acids Oxacyclic compounds Azacyclic compounds Primary amines Hydrocarbon derivatives Primary alcohols Organic oxides

Not available

3'-thia pyrimidine nucleoside - Salicylic acid or derivatives - Salicylic acid - Hydroxybenzoic acid - Benzoic acid - Benzoic acid or derivatives - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Aminopyrimidine - Pyrimidone - Phenol - Hydropyrimidine - Monocyclic benzene moiety - Imidolactam - Benzenoid - Pyrimidine - Heteroaromatic compound - Vinylogous acid - Monothioacetal - Oxathiolane - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary amine - Organonitrogen compound - Organooxygen compound - 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