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Peptidomimetic antibiotic (protegrin-derived)

Murepavadin

Murepavadin (POL7080) is a synthetic cyclic beta-hairpin peptidomimetic derived from the host-defense peptide protegrin I. Unlike broad membrane-lytic peptides, it is Pseudomonas-specific, binding the outer-membrane protein LptD to disrupt lipopolysaccharide transport, and it has been studied against multidrug-resistant Pseudomonas aeruginosa. This page is educational and not medical advice.

By The Peptides Codex Editorial TeamReviewed July 10, 2026
Length
n/a
Class
Peptidomimetic antibiotic (protegrin-derived)
Function
Species-specific inhibitor of LptD in Pseudomonas aeruginosa
Context
Investigational antibiotic studied for Pseudomonas aeruginosa infections

A first-in-class outer-membrane protein target: it binds LptD to block lipopolysaccharide transport in Pseudomonas.

Also known as: POL7080 · RG7929

Part of the Foundational & therapeutic peptides cluster

Overview

Murepavadin (POL7080) is a synthetic cyclic beta-hairpin peptidomimetic derived from the host-defense peptide protegrin I. Unlike broad membrane-lytic peptides, it is Pseudomonas-specific, binding the outer-membrane protein LptD to disrupt lipopolysaccharide transport, and it has been studied against multidrug-resistant Pseudomonas aeruginosa. This page is educational and not medical advice.

Source & context

Biological / chemical source: Synthetic cyclic beta-hairpin peptidomimetic based on protegrin I

Primary research or clinical context: Investigational antibiotic studied for Pseudomonas aeruginosa infections

Novel target

Murepavadin binds LptD, an outer-membrane protein essential for lipopolysaccharide biogenesis in Gram-negative bacteria. This mechanism differs from classic antibiotics and retains activity against many carbapenemase-producing and colistin-resistant Pseudomonas isolates, making it a notable research example of narrow-spectrum, target-specific peptidomimetics.

Development status

Intravenous murepavadin completed phase II studies and entered phase III for hospital-acquired and ventilator-associated pneumonia caused by Pseudomonas aeruginosa. Trials were affected by kidney-toxicity signals, and inhaled formulations have been explored. It is discussed here for scientific context, not as an approved therapy.

FAQ about Murepavadin

What is Murepavadin?+

Murepavadin (POL7080) is a synthetic cyclic beta-hairpin peptidomimetic derived from the host-defense peptide protegrin I. Unlike broad membrane-lytic peptides, it is Pseudomonas-specific, binding the outer-membrane protein LptD to disrupt lipopolysaccharide transport, and it has been studied against multidrug-resistant Pseudomonas aeruginosa. This page is educational and not medical advice.

Is Murepavadin an approved medicine?+

Murepavadin is discussed here as a research / educational topic. Investigational antibiotic studied for Pseudomonas aeruginosa infections. This is not medical advice.

What is the typical length of Murepavadin?+

Murepavadin is not a classic amino-acid chain peptide in the same sense; see the profile for classification details.

Related peptides

References & further reading

  1. 1.Wikipedia — Murepavadin
  2. 2.PubChem — compound summary for Murepavadin (CID 91824766)
Disclaimer: Educational content only. Not medical advice. Not instructions for human use. Research peptides and unapproved products may be restricted or illegal to market for human consumption in your jurisdiction. Consult qualified professionals and applicable law.
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Cite this: Peptides Codex — Murepavadin educational profile.
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