Cc1ccc(cc1)N(\C=N\C1=NC(=O)N(C=C1)C1CSC(CO)O1)c1ccc(C)cc1

InChIKey=KSOPLBGTHVWPGH-BUVRLJJBSA-N

C23H24N4O3S

436.53

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3'-thia pyrimidine nucleosides

Not available

3'-thia pyrimidine nucleosides

Toluenes Pyrimidones Hydropyrimidines Oxathiolanes Monothioacetals Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Formamidines Carboxamidines Azacyclic compounds Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

3'-thia pyrimidine nucleoside - Pyrimidone - Toluene - Monocyclic benzene moiety - Hydropyrimidine - Pyrimidine - Benzenoid - Monothioacetal - Oxathiolane - Heteroaromatic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Azacycle - Organoheterocyclic compound - Oxacycle - Carboxylic acid amidine - Formamidine - Amidine - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Alcohol - Primary alcohol - Organic oxygen compound - Organic nitrogen compound - Organic oxide - 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