Unknown

Dataset Information

0

Synthesis and anti-HSV activity of tricyclic penciclovir and hydroxybutylguanine derivatives.


ABSTRACT: A series of tricyclic penciclovir (PCV) and hydroxybutylguanine (HBG) derivatives have been prepared with enhanced lipophilicity following an efficient synthetic route. All the novel tricyclic derivatives were evaluated for inhibitory activity against herpes simplex virus 1 and 2 (HSV-1, HSV-2) and thymidine kinase deficient (ACV resistant) HSV-1. The tricyclic HBG derivatives were devoid of inhibitory activity however several of the tricyclic PCV derivatives showed promising antiviral activity, in particular 9g (R?=?4-MeO-C6H4) displayed good inhibitory activity (HSV-1 EC50 1.5??M, HSV-2 EC50 0.8??M) and retained inhibitory activity in HSV-1 TK- cells (EC50 0.8??M). Computational docking experiments supported the biological data observed and this preliminary study provides useful data for further development of tricyclic acyclic nucleoside derivatives with improved lipophilicity and retention of activity in HSV-1 TK deficient strains. Also, the new tricyclic derivatives were evaluated against a broad range of other DNA and RNA viruses, but were found to be inactive at subtoxic concentrations. In addition, weak to moderate cytostatic effect was observed for the new compounds.

SUBMITTER: Mohammed AF 

PROVIDER: S-EPMC7126098 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Synthesis and anti-HSV activity of tricyclic penciclovir and hydroxybutylguanine derivatives.

Mohammed Anber F AF   Andrei Graciela G   Hayallah Alaa M AM   Abdel-Moty Samia G SG   Snoeck Robert R   Simons Claire C  

Bioorganic & medicinal chemistry 20190202 6


A series of tricyclic penciclovir (PCV) and hydroxybutylguanine (HBG) derivatives have been prepared with enhanced lipophilicity following an efficient synthetic route. All the novel tricyclic derivatives were evaluated for inhibitory activity against herpes simplex virus 1 and 2 (HSV-1, HSV-2) and thymidine kinase deficient (ACV resistant) HSV-1. The tricyclic HBG derivatives were devoid of inhibitory activity however several of the tricyclic PCV derivatives showed promising antiviral activity,  ...[more]

Similar Datasets

| S-EPMC8346139 | biostudies-literature
| S-EPMC9301648 | biostudies-literature
| S-EPMC5988308 | biostudies-literature
| S-EPMC2748688 | biostudies-literature
| S-EPMC6010105 | biostudies-other
| S-EPMC5592639 | biostudies-literature
| S-EPMC5316254 | biostudies-literature
| S-EPMC6271340 | biostudies-other
| S-EPMC7695678 | biostudies-literature
| S-EPMC4160763 | biostudies-literature