CC1=CC=CC=C1SC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NCCC1=CC=CC=C1

InChIKey=FYTGTZKRXSZVNR-PXOHRUDZSA-N

C25H27N5O3S

477.58

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

5'-deoxy-5'-thionucleosides

Not available

5'-deoxy-5'-thionucleosides

6-alkylaminopurines Glycosylamines Pentoses Thiophenol ethers Toluenes Alkylarylthioethers Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Heteroaromatic compounds Oxolanes 1,2-diols Secondary alcohols Sulfenyl compounds Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Amines

Aromatic heteropolycyclic compounds

5'-deoxy-5'-thionucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Thiophenol ether - Aryl thioether - Aminopyrimidine - Alkylarylthioether - Toluene - Imidolactam - Benzenoid - N-substituted imidazole - Monosaccharide - Monocyclic benzene moiety - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Oxolane - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organic nitrogen compound - Alcohol - Amine - Organic oxygen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as 5'-deoxy-5'-thionucleosides. These are 5'-deoxyribonucleosides in which the ribose is thio-substituted at the 5'position by a S-alkyl group.

Not available