Triazolopyrimidines and Thiazolopyrimidines: Synthesis, Anti-HSV-1, Cytotoxicity and Mechanism of Action

Title:Triazolopyrimidines and Thiazolopyrimidines: Synthesis, Anti-HSV-1, Cytotoxicity and Mechanism of Action

Volume: 18 Issue: 9

Author(s): Salwa F. Mohamed, Eman M.H. Abbas, Hemat S. Khalaf, Thoraya A. Farghaly*Dina N. Abd El-Shafy

Affiliation:

• Department of Chemistry, Faculty of Science, Cairo University, Giza 12613,Egypt

Keywords: Thiazolopyrimidine, triazolopyrimidine, hydrazonoyl halides, anti-HSV-1, mechanism of action, spectroscopic.

Abstract: Background: Several commercial drugs utilized in the treatment of HSV containing pyrimidine moiety. Because of the ineffectiveness of virus drugs due to the resistance of the patient's immune system, there is a pressing need to prepare new compounds that are effective in the treatment of various viruses.

Results: Merged pyrimidine derivatives were designed by one pot synthesis of pyrimidinethione derivative with halogenated compounds. The structure of all prepared compounds was characterized by their spectroscopic data and also, their ability to inhibit the in vitro replication of HSV-1 was estimated. Amongst the tested compounds 2-acetyl-3-methyl-5-(p-tolyl)indeno[1,2-d]thiazolo[3,2- a]pyrimidin-6(5H)-one (9b) and ethyl 3-methyl-6-oxo-5-(p-tolyl)-5,6-dihydroindeno[1,2-d]thiazolo- [3,2-a]pyrimidine-2-carboxylate (9c), caused viral inhibition over 90%. Furthermore, the selectivity indices of the tested compounds are high and have weak cytotoxicity (all samples were checked, not chosen on cytotoxicity basis, we only utilize secure concentrations of every compound).

Conclusion: We succeeded in this context to synthesize a new series of potent fused pyrimidine derivatives as anti-HSV-1.

Cite this article as:

Mohamed F. Salwa , Abbas M.H. Eman , Khalaf S. Hemat, Farghaly A. Thoraya*, Abd El-Shafy N. Dina, Triazolopyrimidines and Thiazolopyrimidines: Synthesis, Anti-HSV-1, Cytotoxicity and Mechanism of Action, Mini-Reviews in Medicinal Chemistry 2018; 18 (9) . https://dx.doi.org/10.2174/1389557518666171207161542