CSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)nc(N=[N+]=[N-])nc12

InChIKey=AXDXDYYJJJSSHU-KQYNXXCUSA-N

C11H14N8O3S

338.35

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

5'-deoxy-5'-thionucleosides

Not available

5'-deoxy-5'-thionucleosides

Glycosylamines Pentoses Imidazopyrimidines Aryl azides Pyrimidines and pyrimidine derivatives N-substituted imidazoles Imidolactams Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Organic azides Sulfenyl compounds Oxacyclic compounds Dialkylthioethers Azacyclic compounds Primary amines Organopnictogen compounds Organic zwitterions Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

5'-deoxy-5'-thionucleoside - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Aryl azide - Imidazopyrimidine - Imidolactam - Pyrimidine - N-substituted imidazole - Monosaccharide - Heteroaromatic compound - Tetrahydrofuran - Azole - Organoazide - Secondary alcohol - Organic azide - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkylthioether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Thioether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic zwitterion - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Amine - 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