NC1=NC(=O)N(C=C1)[C@@H]1CS[C@H](CO)O1.CC(C)=CCOC1=C(Cl)C=CC(NC(=S)C2=C(C)OC=C2)=C1

InChIKey=WTDJORSDUWIORZ-HLISZSCWSA-N

C25H29ClN4O5S2

565.1

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3'-thia pyrimidine nucleosides

Not available

3'-thia pyrimidine nucleosides

Phenoxy compounds Phenol ethers Alkyl aryl ethers Pyrimidones Aminopyrimidines and derivatives Chlorobenzenes Hydropyrimidines Imidolactams Primary aromatic amines Aryl chlorides Heteroaromatic compounds Furans Thioamides Oxathiolanes Monothioacetals Thiocarboxylic acid amides Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organochlorides Organopnictogen compounds Primary alcohols Thiocarbonyl compounds

Not available

3'-thia pyrimidine nucleoside - Phenoxy compound - Phenol ether - Alkyl aryl ether - Aminopyrimidine - Chlorobenzene - Halobenzene - Pyrimidone - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - Imidolactam - Benzenoid - Primary aromatic amine - Pyrimidine - Heteroaromatic compound - Furan - Monothioacetal - Oxathiolane - Thioamide - Organoheterocyclic compound - Thiocarboxylic acid amide - Ether - Oxacycle - Azacycle - Thiocarbonyl group - Organochloride - Organohalogen compound - Amine - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organosulfur compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary alcohol - Primary amine - Organic oxygen compound - 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