# Virtual Screening of Marine Natural Products Targeting the F Protein for Anti-RSV Drug Discovery

**Authors:** Wenqing Liu, Xuran Gu, Ruikun Du, Zhiqing Liu, Pingyuan Wang, Chang-Yun Wang

PMC · DOI: 10.3390/ijms27052484 · International Journal of Molecular Sciences · 2026-03-08

## TL;DR

This study uses virtual screening to find marine natural products that could inhibit RSV by targeting its F protein, with manzamine alkaloids showing strong potential.

## Contribution

The study introduces marine natural products, particularly manzamine alkaloids, as novel leads for RSV fusion inhibitors.

## Key findings

- 11 promising compounds were identified from 31,561 marine natural products via virtual screening and ADMET profiling.
- Manzamine alkaloids showed the best docking scores and favorable interactions with conserved residues on the F protein.
- The compounds interact through hydrophobic, π-stacking, and electrostatic interactions with the F protein.

## Abstract

Respiratory syncytial virus (RSV) poses a substantial global health burden, particularly in infants and the elderly. The fusion (F) protein is a key therapeutic target for inhibiting RSV entry. In this study, we performed a structure-based virtual screening of the Comprehensive Marine Natural Products Database (CMNPD) to discover novel anti-RSV agents targeting the prefusion F protein trimer. Screening of 31,561 compounds via molecular docking, followed by stringent ADMET (absorption, distribution, metabolism, excretion, and toxicity) profiling and MM/GBSA (Molecular Mechanics/Generalized Born Surface Area) binding free energy calculations, identified 11 promising candidates. Among these, manzamine alkaloids exhibited the most favorable docking scores (as low as −13.3 kcal/mol) and promising Ligand Efficiency (LE) values. These molecules primarily interact with conserved hydrophobic residues (Phe140, Phe488) through hydrophobic interactions, π-stacking, and electrostatic forces. Our study highlights marine natural products, especially manzamine alkaloids, as promising leads for the development of novel, orally bioavailable RSV fusion inhibitors, potentially offering avenues to overcome existing drug resistance. However, these computational findings require in vitro validation to confirm efficacy.

## Linked entities

- **Proteins:** f-protein (F-protein)

## Full-text entities

- **Diseases:** toxicity (MESH:D064420)
- **Chemicals:** manzamine alkaloids (-)
- **Species:** Respiratory syncytial virus (no rank) [taxon 12814]

## Full text

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## Figures

50 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12985475/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12985475/full.md

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Source: https://tomesphere.com/paper/PMC12985475