CSC1=NC2=C(N=CN2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(NCC2=CC(Cl)=CC=C2)=N1

InChIKey=RVZNORGBJQOMHL-LSCFUAHRSA-N

C18H20ClN5O4S

437.9

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-alkylaminopurines Glycosylamines Pentoses Benzylamines Alkylarylthioethers Aminopyrimidines and derivatives Chlorobenzenes Aryl chlorides N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Secondary alcohols Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Primary alcohols Organochlorides Amines Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aryl thioether - Benzylamine - Aminopyrimidine - Chlorobenzene - Halobenzene - Alkylarylthioether - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Imidolactam - Monosaccharide - N-substituted imidazole - Benzenoid - Pyrimidine - Azole - Oxolane - Heteroaromatic compound - Imidazole - Secondary alcohol - Thioether - Sulfenyl compound - Oxacycle - Organoheterocyclic compound - Azacycle - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Amine - Organosulfur compound - Organic nitrogen compound - Alcohol - Primary alcohol - Organohalogen compound - Organochloride - Organonitrogen 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