CCCNC(=S)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(Cl)N=C3NC2CCCC2)[C@](C)(O)[C@@H]1O

InChIKey=UYHXBFMNMPXEII-DPBUJNAFSA-N

C20H29ClN6O4S

485.0

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-alkylaminopurines Glycosylamines Pentoses 2-halopyrimidines Secondary alkylarylamines Aminopyrimidines and derivatives Aryl chlorides Imidolactams N-substituted imidazoles Thiocarbamic acid esters Heteroaromatic compounds Oxolanes Tertiary alcohols 1,2-diols Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organochlorides

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Purine - Imidazopyrimidine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Secondary aliphatic/aromatic amine - N-substituted imidazole - Monosaccharide - Imidolactam - Aryl halide - Pyrimidine - Aryl chloride - Heteroaromatic compound - Azole - Imidazole - Thiocarbamic acid ester - Tertiary alcohol - Oxolane - Secondary alcohol - 1,2-diol - Thiocarbamic acid derivative - Secondary amine - Oxacycle - Azacycle - Organoheterocyclic compound - Organochloride - Alcohol - Amine - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - 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