CC1=CC=CC=C1SC[C@H]1OC([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NC1CCOC1

InChIKey=ONRJXNKUWBFJQE-AJLQVLIESA-N

C21H25N5O4S

443.52

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

5'-deoxy-5'-thionucleosides

Not available

5'-deoxy-5'-thionucleosides

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

Aromatic heteropolycyclic compounds

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