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Updated: Oct 17, 2026

Nucleoside Triphosphates - From Synthesis to Biochemical Characterization
Published on: April 3, 2014
Design, synthesis, conformational analysis and biological activities of purine-based 1,2-di-substituted carbocyclic
C Teran1, L Santana, M Teijeira
1Departamento de Química Física y Química Orgánica, Universidad de Vigo, Spain.
Abstract:
New 1,2-di-substituted carbocyclic nucleosides with 6-chloropurine, adenine and hypoxanthine bases were synthesized by construction of purine on the primary amino group of (+/-)-trans-2-aminocyclopentylmethanol. AM1 calculations showed close correspondence between the positions of the heteroatoms in the adenine derivative and dideoxyadenosine. The most active of the new compounds in antiviral assays and antitumoral assays against L1210/0, MOLT4/C8 and CEM/0 cells was the 6-chloropurine derivative.
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