Cl.NC1=NC(SC2CN3CCC2CC3)=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

InChIKey=NBJPVCAGXPZGHI-KDXJJXABSA-N

C17H25ClN6O4S

444.94

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-aminopurines Pentoses Quinuclidines Alkylarylthioethers Aminopyrimidines and derivatives Piperidines N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Trialkylamines Secondary alcohols Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Hydrochlorides Organopnictogen compounds Primary alcohols Primary amines

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aryl thioether - Quinuclidine - Aminopyrimidine - Alkylarylthioether - Monosaccharide - N-substituted imidazole - Piperidine - Pyrimidine - Imidolactam - Azole - Oxolane - Imidazole - Heteroaromatic compound - Secondary alcohol - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Sulfenyl compound - Azacycle - Thioether - Oxacycle - Organic oxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Primary alcohol - Primary amine - Hydrochloride - 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