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

InChIKey=DQBMXDWVUYSFGY-DPBUJNAFSA-N

C20H29ClN6O5

468.94

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 Aryl chlorides Tertiary alcohols Oxolanes Heteroaromatic compounds Carbamate esters Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds Organochlorides

Aromatic heteropolycyclic compounds

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