Keywords

Chalcones, Antiviral, Viruses

Abstract

Chalcones are a class of compounds naturally found in plants and are predicated upon a 1,3-diphenylprop-2-en-1-one scaffold. Chalcones possess many biological activities ranging from anticancer to antiviral activities. This thesis investigates the broad-spectrum antiviral properties of chalcones. Some chalcones have been reported to affect host cell mechanisms such as mammalian target of rapamycin (mTOR) signaling cascade or the cell cycle to reduce viral replication. Previously, a series of chalcones 8 were synthesized and investigated in human cytomegalovirus virus (HCMV) and human immunodeficiency virus (HIV). In this study, ten new chalcones predicated upon the design of 8 were synthesized and a possible mechanism of action and antiviral properties were investigated. The chalcones were synthesized via a cross-aldol condensation reaction. Next, the MTS assay was used to determine the relative growth inhibition of each chalcone and to calculate their EC10 and EC50 values. In CHO-K1 hamster ovary cells, Hs27 human fibroblast cells and PANC-1 human pancreatic cancer cells, chalcones 8a and LK6 were the least growth inhibitory as evidenced by their higher EC50 values. The phenotypical changes and the relative cell-count changes in Hs27 cells (treated with chalcones at their EC50 value over 48 h) were determined. All chalcones tested had cell counts below the untreated control indicating their ability to inhibit proliferation. In PANC-1 cells the effect on mTOR signaling with select chalcones was determined. Most of the chalcones showed no significant difference in P-rps6 and rps6 protein expression suggesting that mTOR is not the target of these compounds. Finally, the effect of chalcones on viral replication was assessed. Compound 8o showed inhibition of viral replication and protein expression in Parainfluenza 5 virus (PIV5), La Crosse virus (LACV), Zika virus (ZIKV) and Coronavirus (OC43)-infected cells. A balance between toxicity and antiviral activity was achieved by chalcone 8o which may serve as a potential pan antiviral.

Completion Date

2025

Semester

Summer

Committee Chair

Otto Phanstiel. Ph.D

Degree

Master of Science (M.S.)

College

College of Medicine

Department

Burnett School of Biomedical Science

Format

PDF

Release Date

8-15-2026

Document Type

Thesis

Subjects

Plant antiviral agents; Antiviral agents--Testing; Virus inhibitors--Testing; Viruses--Research; Viruses--Effect of drugs on

Available for download on Saturday, August 15, 2026

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