Kumar, Vipul and Sari, Anissa Nofita and Gupta, Dharmender and Ishida, Yoshiyuki and Terao, Keiji and Kaul, Sunil C. and Vrati, Sudhanshu and Sundar, Durai and Wadhwa, Renu (2024) Anti-COVID-19 Potential of Withaferin-A and Caffeic Acid Phenethyl Ester. Current Topics in Medicinal Chemistry, 24 (9). pp. 830-842. ISSN 15680266
Full text not available from this repository. (Request a copy)Abstract
Background:
The recent COVID-19 (coronavirus disease 2019) pandemic triggered research on the development of new vaccines/drugs, repurposing of clinically approved drugs, and assessment of natural anti-COVID-19 compounds. Based on the gender difference in the severity of the disease, such as a higher number of men hospitalized and in intense care units, variations in sex hormones have been predicted to play a role in disease susceptibility. Cell surface receptors (Angiotensin-Converting Enzyme 2; ACE2 and a connected transmembrane protease serine 2- TMPSS2) are upregulated by androgens. Conversely, androgen antagonists have also been shown to lower ACE2 levels, implying their usefulness in COVID-19 management.
Objective:
In this study, we performed computational and cell-based assays to investigate the anti- COVID-19 potential of Withaferin-A and Caffeic acid phenethyl ester, natural compounds from Withania somnifera and honeybee propolis, respectively
Methods:
Structure-based computational approach was adopted to predict binding stability, interactions, and dynamics of the two test compounds to three target proteins (androgen receptor, ACE2, and TMPRSS2). Further, in vitro, cell-based experimental approaches were used to investigate the effect of compounds on target protein expression and SARS-CoV-2 replication.
Results:
Computation and experimental analyses revealed that (i) CAPE, but not Wi-A, can act as androgen antagonist and hence inhibit the transcriptional activation function of androgen receptor, (ii) while both Wi-A and CAPE could interact with ACE2 and TMPRSS2, Wi-A showed higher binding affinity, and (iii) combination of Wi-A and CAPE (Wi-ACAPE) caused strong downregulation of ACE2 and TMPRSS2 expression and inhibition of virus infection.
Conclusion:
Wi-A and CAPE possess multimodal anti-COVID-19 potential, and their combination (Wi-ACAPE) is expected to provide better activity and hence warrant further attention in the laboratory and clinic.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Withaferin-A, Caffeic acid phenethyl ester, SARS-CoV-2, Androgen Receptor (AR), Transmembrane Protease Serine 2 (TMPRSS2), Angiotensin Converting Enzyme 2 (ACE2). |
| Subjects: | Medicine & Biology |
| Depositing User: | Maria Regina Karunia |
| Date Deposited: | 09 Jun 2026 03:30 |
| Last Modified: | 09 Jun 2026 03:30 |
| URI: | https://karya.brin.go.id/id/eprint/58646 |


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