Design and Synthesis of Novel 1′,3′-Dioxolane 5′-Deoxyphosphonic Acid Purine Analogues as Potent Antiviral Agents
摘要:
Electronic parameters of 1',3'-oxygen play significant roles in steering the conformation of nucleoside phosphonic acid analogues. To investigate the relationship of two oxygen atoms with antiviral enhancement, novel. 1',3'-dioxolane 5'-deoxyphosphonic acid purine analogues were synthesized via de novo acyclic stereoselective route from acrolein and glycolic acid. The synthesized nucleoside phosphonic acid analogues 19 and 19 were subjected to antiviral screening against several viruses, such. as HIV-1, HSV-1, HSV-2, and HCMV The guanine analogue 19 exhibits in vitro anti-HIV-1 activity similar to that of 9[2-(phosphonomethoxy)ethyl]adenine (PMEA) in MT-4 cells.
Design and Synthesis of Novel 1′,3′-Dioxolane 5′-Deoxyphosphonic Acid Purine Analogues as Potent Antiviral Agents
摘要:
Electronic parameters of 1',3'-oxygen play significant roles in steering the conformation of nucleoside phosphonic acid analogues. To investigate the relationship of two oxygen atoms with antiviral enhancement, novel. 1',3'-dioxolane 5'-deoxyphosphonic acid purine analogues were synthesized via de novo acyclic stereoselective route from acrolein and glycolic acid. The synthesized nucleoside phosphonic acid analogues 19 and 19 were subjected to antiviral screening against several viruses, such. as HIV-1, HSV-1, HSV-2, and HCMV The guanine analogue 19 exhibits in vitro anti-HIV-1 activity similar to that of 9[2-(phosphonomethoxy)ethyl]adenine (PMEA) in MT-4 cells.
Design and Synthesis of Novel 1′,3′-Dioxolane 5′-Deoxyphosphonic Acid Purine Analogues as Potent Antiviral Agents
作者:Eunae Kim、Lian Jin Liu、Wonjae Lee、Joon Hee Hong
DOI:10.1080/15257770.2011.643849
日期:2012.2
Electronic parameters of 1',3'-oxygen play significant roles in steering the conformation of nucleoside phosphonic acid analogues. To investigate the relationship of two oxygen atoms with antiviral enhancement, novel. 1',3'-dioxolane 5'-deoxyphosphonic acid purine analogues were synthesized via de novo acyclic stereoselective route from acrolein and glycolic acid. The synthesized nucleoside phosphonic acid analogues 19 and 19 were subjected to antiviral screening against several viruses, such. as HIV-1, HSV-1, HSV-2, and HCMV The guanine analogue 19 exhibits in vitro anti-HIV-1 activity similar to that of 9[2-(phosphonomethoxy)ethyl]adenine (PMEA) in MT-4 cells.