CC(CCC1=CC=CC=C1)NC1=NC(Cl)=NC2=C1N=CN2[C@@H]1O[C@H](CO)C(O)C1O

InChIKey=LRMPVYGAYJKNJT-VCJLRBCGSA-N

C20H24ClN5O4

433.89

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

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

Aromatic heteropolycyclic compounds

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