CC1=CC=C(C=C1)S(=O)(=O)N1[C@@H]2[C@H]1[C@H](C[C@H]2CO)N1C=NC2=C1N=CN=C2Cl

InChIKey=WGZHEQQCGZAEOZ-URTCHXBBSA-N

C18H18ClN5O3S

419.88

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Cyclopentyl nucleosides

1,3-substituted cyclopentyl nucleosides

1,3-substituted cyclopentyl purine nucleosides

N,N-disubstituted p-toluenesulfonamides Benzenesulfonamides Purines and purine derivatives Benzenesulfonyl compounds Halopyrimidines Aryl chlorides Piperidines Organosulfonamides N-substituted imidazoles Heteroaromatic compounds Sulfonyls Aziridines Azacyclic compounds Hydrocarbon derivatives Primary alcohols Organic oxides Organochlorides Organonitrogen compounds

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - N,n-disubstituted p-toluenesulfonamide - P-toluenesulfonamide - Benzenesulfonamide - Tosyl compound - Imidazopyrimidine - Purine - Benzenesulfonyl group - Halopyrimidine - Toluene - N-substituted imidazole - Aryl chloride - Benzenoid - Monocyclic benzene moiety - Piperidine - Organosulfonic acid amide - Aryl halide - Pyrimidine - Imidazole - Heteroaromatic compound - Azole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aziridine - Organoheterocyclic compound - Azacycle - Organic oxide - Organohalogen compound - Alcohol - Organochloride - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Primary alcohol - Organic oxygen compound - Hydrocarbon derivative - 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