# PoMA-10: a dual-action antiviral disrupting SARS-CoV-2 Spike–ACE2 interaction and protecting lung tissue

**Authors:** Soheun Lee, Suh Jin Yoon, Jihae Lim, Ji Hyun Oh, Jae-Sang Ryu, Gahee Kim, Hyunwoo Kang, Nayoon Jo, Sehan Lee, Sunbok Jang, Yoonji Lee, Yunjeong Park, Eun Sook Hwang

PMC · DOI: 10.3389/fphar.2026.1755268 · Frontiers in Pharmacology · 2026-03-12

## TL;DR

This study identifies PoMA-10, a compound that blocks SARS-CoV-2 from entering cells and protects lung tissue, offering a potential treatment for COVID-19.

## Contribution

PoMA-10 is a novel dual-action antiviral that inhibits Spike-ACE2 interaction while preserving ACE2 function and protecting lung tissue.

## Key findings

- PoMA-10 effectively inhibits SARS-CoV-2 Spike-ACE2 interaction without impairing ACE2 activity.
- PoMA-10 reduces infection by SARS-CoV-2 variants and protects against lung injury in vivo.
- Computational and experimental methods confirmed PoMA-10's stable binding to ACE2.

## Abstract

This study aimed to identify small molecules that inhibit the binding of the SARS-CoV-2 Spike protein to its host receptor, angiotensin-converting enzyme 2 (ACE2), without impairing the enzymatic activity of ACE2. Such inhibitors may support the development of broad-spectrum antivirals and therapeutic strategies for emerging SARS-CoV-2 variants. Through extensive screening using both cell-free and cell-based assays, we identified phenoxy-methylaniline (PoMA) compounds as effective inhibitors of the SARS-CoV-2 Spike-ACE2 interaction. Among these, PoMA-10, featuring trifluoromethoxy and dimethylaniline moieties, exhibited the most potent inhibitory activity while preserving ACE2 enzymatic function. Computational modeling predicted direct binding of PoMA-10 to ACE2, which was corroborated by protein mobility shift assays. This was further substantiated by surface plasmon resonance analysis and molecular dynamics simulations, which confirmed the stable binding of PoMA-10 at an interface-adjacent site on ACE2 and the disruption of SARS-CoV-2 Spike–ACE2 interaction. In Vero cells, PoMA-10 significantly reduced infection by ancestral SARS-CoV-2 and the Delta and Gamma variants. Moreover, PoMA-10 alleviated lung epithelial cell damage and protected against lipopolysaccharide-induced lung injury in vivo. These findings demonstrate that PoMA-10 functions as a dual-action inhibitor blocking viral entry and protecting against lung injury, and highlight its potential as a therapeutic candidate in the management of COVID-19 and related pulmonary complications.

## Linked entities

- **Proteins:** ACE2 (angiotensin converting enzyme 2)
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Diseases:** infection (MESH:D007239), pulmonary complications (MESH:D008171), lung injury (MESH:D055370), COVID-19 (MESH:D000086382)
- **Chemicals:** PoMA (-), lipopolysaccharide (MESH:D008070)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13017958/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC13017958/full.md

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Source: https://tomesphere.com/paper/PMC13017958