CC1(C)O[C@@H]2[C@H](O1)[C@]1(CO)C[C@@H]1[C@H]2N1C=NC2=C1N=C(Cl)N=C2N

InChIKey=JGPIEHIXFNKRCS-RFXZSQAESA-N

C15H18ClN5O3

351.79

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Cyclopentyl nucleosides

1,3-substituted cyclopentyl nucleosides

1,3-substituted cyclopentyl purine nucleosides

6-aminopurines 2-halopyrimidines Aminopyrimidines and derivatives Ketals Primary aromatic amines Aryl chlorides Imidolactams N-substituted imidazoles Heteroaromatic compounds 1,3-dioxolanes Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Primary alcohols Organopnictogen compounds Organochlorides

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Ketal - Imidolactam - Pyrimidine - N-substituted imidazole - Aryl halide - Aryl chloride - Primary aromatic amine - Azole - Imidazole - Meta-dioxolane - Heteroaromatic compound - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Primary alcohol - Primary amine - Alcohol - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Organooxygen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as 1,3-substituted cyclopentyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3-position with either a purine base.

Not available