NC1=NC(=O)N(C=C1)[C@@H]1CS[C@H](CO)O1.C\C(=N/N=C(N)N)C1=CC(=CC(NC(=O)CCCCCCCCC(=O)NC2=CC(=CC(=C2)C(\C)=N\N=C(N)N)C(\C)=N\N=C(N)N)=C1)C(\C)=N\N=C(N)N

InChIKey=RCSLFODXQHYUMJ-FNMJLNBNSA-N

C42H63N21O5S

974.17

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3'-thia pyrimidine nucleosides

Not available

3'-thia pyrimidine nucleosides

Anilides N-arylamides Aminopyrimidines and derivatives Pyrimidones Fatty amides Hydropyrimidines Imidolactams Monothioacetals Heteroaromatic compounds Oxathiolanes Guanidines Secondary carboxylic acid amides Azacyclic compounds Oxacyclic compounds Primary alcohols Primary amines Hydrocarbon derivatives Carbonyl compounds Organic oxides

Not available

3'-thia pyrimidine nucleoside - Anilide - N-arylamide - Aminopyrimidine - Pyrimidone - Monocyclic benzene moiety - Fatty amide - Hydropyrimidine - Pyrimidine - Benzenoid - Imidolactam - Fatty acyl - Heteroaromatic compound - Oxathiolane - Monothioacetal - Secondary carboxylic acid amide - Carboxamide group - Guanidine - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Alcohol - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Amine - Primary alcohol - Hydrocarbon derivative - Carbonyl group - Primary amine - Organic oxygen 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