The COVID-19 pandemic has highlighted the critical need for effective antiviral therapies, as viral infections remain a leading cause of mortality worldwide. Natural compounds, especially those derived from plants, have been recognized for their therapeutic properties. Ginseng, in particular, has attracted considerable attention for its potential antiviral effects. This review examines the antiviral compounds from ginseng that act against various human pathogenic viruses. We systematically summarize the antiviral activities of ginseng compounds targeting a range of viruses, including human rhinovirus (HRV), influenza virus, human immunodeficiency virus (HIV), hepatitis viruses A, B, and C (HAV, HBV, HCV), herpes simplex virus (HSV), enterovirus 71 (EV71), coxsackievirus, norovirus, and SARS-CoV-2, the virus responsible for COVID-19. This review covers , , and , discussing their mechanisms of action and therapeutic potential. The analysis incorporates literature from February 2002 through August 2024, providing a comprehensive overview of the existing evidence on the antiviral properties of compounds derived from ginseng. This review aims to underscore the scientific basis for developing ginseng as an antiviral therapeutic agent or nutraceutical.
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http://dx.doi.org/10.1016/j.jgr.2024.12.004 | DOI Listing |
Phys Chem Chem Phys
March 2025
Ivanovo State University of Chemistry and Technology, Department of Physical and Colloidal Chemistry, Sheremetevskiy Ave, 7, 153000 Ivanovo, Russia.
A gas-phase electron diffraction analysis combined with mass-spectrometry (GED/MS) of (2,9)--2,9-diiodo-13-(triflyl)-13-azabicyclo[8.2.1]tridec-5-ene was performed and the results were compared with those studied earlier by GED/MS and X-ray analysis of triflamide derivatives, that is 3,7,9-tris(triflyl)-3,7,9-triazabicyclo[3.
View Article and Find Full Text PDFChem Rec
March 2025
Department of Chemistry, CMS College Kottayam (Autonomous), Kerala, 686001, India.
Organofluorine compounds are of pivotal significance particularly, in drug and agrochemical industries and different strategies have been designed for their synthesis. The last two decades witnessed the emergence of difluorocarbene as an efficient synthetic tool, providing easy access to organofluorine compounds. This review summarises the reactions of difluorocarbene generated from Ruppert-Prakash reagent (TMSCF) and its derivatives TMSCFCl and TMSCFBr.
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February 2025
Medicinal Chemistry Unit, School of Pharmacy, University of Camerino, Via Madonna delle Carceri, I-62032 Camerino, Italy.
Parkinson's disease (PD) represents a growing challenge to global health, as it involves millions of people. The high grade of disability is due to the loss of dopaminergic neuron activity, and levodopa is the gold-standard therapy used to restore dopamine in the dopamine-denervated regions. Another therapeutic approach is the use of A adenosine receptor antagonists and, among them, istradefylline is the only one currently approved for therapy in association with levodopa.
View Article and Find Full Text PDFNat Prod Res
March 2025
Fermentation and Microbial Biotechnology Division, CSIR - Indian Institute of Integrative Medicine, Jammu, India.
A new obscurolide, (3 )-obscurolide A () and four previously identified metabolites streptalbonin F (), chartreusin (), TAN 1364B () and streptalbonin G () were isolated from SA-7, obtained from soil of the North Western Himalayas. The structure of new compound (3 )-obscurolide A () was elucidated by spectroscopic data analysis, including 1D and 2D NMR, and HR-ESI-MS, while the known compounds (-) were identified by comparing their spectral data with the literature. Notably, chartreusin () is a well-known antimicrobial agent with broad-spectrum activity, while the other compounds had been reported to display moderate antimicrobial effects against various test strains.
View Article and Find Full Text PDFArch Pharm (Weinheim)
March 2025
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Bezmialem Vakif University, Istanbul, Türkiye.
This study investigates the anticholinesterase (acetylcholinesterase [AChE] and butyrylcholinesterase [BChE]) and carbonic anhydrase (CAI and CAII) inhibitory activities of carnosic acid and its natural derivatives, including carnosol, rosmanol, 7-methoxy-rosmanol, 12-methoxy-carnosic acid, and isorosmanol. Among the tested compounds, rosmanol demonstrated exceptional potency, with IC values of 0.73 nM for AChE and 0.
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