NC1=NC2=C(N=CN2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(SCC2=CC(Br)=CC=C2)=N1

InChIKey=BOCNNJJYEVIUDP-XNIJJKJLSA-N

C17H18BrN5O4S

468.33

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-thiopurines Pentoses Alkylarylthioethers Aminopyrimidines and derivatives Bromobenzenes Aryl bromides N-substituted imidazoles Oxolanes Heteroaromatic compounds 1,2-diols Secondary alcohols Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Primary alcohols Primary amines Hydrocarbon derivatives Organobromides

Aromatic heteropolycyclic compounds

Purine nucleoside - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - 6-thiopurine - Imidazopyrimidine - Purine - Aryl thioether - Aminopyrimidine - Halobenzene - Bromobenzene - Alkylarylthioether - Pyrimidine - Aryl halide - Aryl bromide - Monosaccharide - N-substituted imidazole - Monocyclic benzene moiety - Benzenoid - Azole - Heteroaromatic compound - Oxolane - Imidazole - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Primary alcohol - Primary amine - Organic oxygen compound - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

Not available