Enzyme-Based Antiviral Potential of Cinnamomum verum J. Presl. Essential Oil and Its Major Component ( E )-Cinnamaldehyde.
Ayşe Esra KaradaǧSevde Nur Biltekin KaleliUsman GhaniBetül DemirciFatih DemirciPublished in: ACS omega (2024)
In the present study, Cinnamomum verum J. Presl. bark essential oil and its main component cinnamaldehyde was evaluated in vitro for neuraminidase (NA), transmembrane serine protease (TMPRSS2), and angiotensin converting enzyme 2 (ACE2) inhibitory activities. The chemical composition of C. verum essential oil was confirmed by both gas chromatography-mass spectrometry (GC/MS), and gas chromatography-flame ionization detection (GC-FID), where 75.9% ( E )-cinnamaldehyde was the major component. The ACE2, NA, and TMPRSS2 enzyme inhibitions of C. verum bark essential oil at 20 μg/mL concentration, and ( E )-cinnamaldehyde (5 μg/mL) were calculated and compared in the range of 54.2-89.9%. Molecular docking results supported that ( E )-cinnam-aldehyde was specific to ACE2 with 89.9% inhibition. Our findings suggest further in vivo studies to confirm the effective and safe use of the essential oil as well as the ( E )-cinnamaldehyde.
Keyphrases
- essential oil
- gas chromatography
- angiotensin converting enzyme
- gas chromatography mass spectrometry
- angiotensin ii
- mass spectrometry
- molecular docking
- tandem mass spectrometry
- high resolution mass spectrometry
- solid phase extraction
- liquid chromatography
- climate change
- high resolution
- protein kinase
- quantum dots
- human health