C[C@H](CNC1=C2N=CN([C@@H]3O[C@H](CO)[C@H](O)[C@H]3O)C2=NC(Cl)=N1)OC1=CC=CC=C1

InChIKey=XVAJVUPAVAOMPL-FXBUUWJESA-N

C19H22ClN5O5

435.87

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-alkylaminopurines Glycosylamines Pentoses Phenoxy compounds Phenol ethers 2-halopyrimidines Alkyl aryl ethers Aminopyrimidines and derivatives Aryl chlorides Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes Secondary alcohols Azacyclic compounds Oxacyclic compounds Organochlorides Amines Hydrocarbon derivatives Primary alcohols

Aromatic heteropolycyclic compounds

Purine nucleoside - N-glycosyl compound - Glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Phenoxy compound - Phenol ether - Alkyl aryl ether - 2-halopyrimidine - Aminopyrimidine - Halopyrimidine - Monosaccharide - N-substituted imidazole - Aryl chloride - Aryl halide - Imidolactam - Pyrimidine - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Imidazole - Azole - Oxolane - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Amine - Primary alcohol - Organic oxygen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - 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