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Cyclic lipopeptide antibiotic

Colistin

Colistin, also called polymyxin E, is a cyclic lipopeptide antibiotic from Paenibacillus species and a close relative of polymyxin B.

By The Peptides Codex Editorial TeamIndividual review date not recorded

Page data last changed: . Chemistry registry snapshot: . Registry refreshes and identity assessments are separate from scientific content review.

Length
n/a
Class
Cyclic lipopeptide antibiotic
Function
Binds lipid A and permeabilizes the Gram-negative outer membrane
Context
Last-resort approved antibiotic for multidrug-resistant Gram-negative infections

Polymyxin E — a last-resort agent whose plasmid-borne mcr-1 resistance gene raised global alarm.

Also known as: polymyxin E · colistimethate (prodrug)

Part of the Foundational & therapeutic peptides cluster

Overview

Colistin, also called polymyxin E, is a cyclic lipopeptide antibiotic from Paenibacillus species and a close relative of polymyxin B. It displaces divalent cations from lipopolysaccharide phosphate groups, breaking down the Gram-negative outer membrane. Classified by the WHO as critically important and reserved as a last-resort drug, its usefulness is threatened by the mobile mcr-1 resistance gene. This page is educational and not medical advice.

Source & context

Biological / chemical source: Bacteria of the genus Paenibacillus (Paenibacillus polymyxa)

Primary research or clinical context: Last-resort approved antibiotic for multidrug-resistant Gram-negative infections

How it works

Like polymyxin B, colistin is a polycationic cyclic lipopeptide rich in diaminobutyric acid. It competitively displaces Ca2+ and Mg2+ that bridge neighboring lipopolysaccharide molecules, destabilizing the outer membrane and causing leakage and death of Gram-negative bacteria. It is administered as the less-toxic prodrug colistimethate sodium.

Resistance concern

Discovered in 1947, colistin was sidelined by toxicity, then revived against carbapenem-resistant organisms. The 2015 discovery of the plasmid-borne mcr-1 gene, which spreads colistin resistance between bacteria, made stewardship of this last-resort drug a major public-health topic.

Structure & chemistry

Molecular identity & reference confidence

Source-supported reference

Reference values are taken from the cited molecular record or curated profile. A database match is not independent laboratory verification; modifications, counter-ions, and formulations can change the measured mass.

Molecular form
Colistin (source record; form not independently established)
Species
Not established by this molecular identity audit
Termini (N / C)
Not specified / Not specified

Average reference mass

Reference policy updated: 2026-10-05

Molecular formula
C52H98N16O13
Average reference mass
≈ 1,155.4
Status
Approved medicine in at least one jurisdiction (IUPHAR record)
Identifiers

Chemistry values: PubChem, IUPHAR/BPS Guide to Pharmacology · fetched 2026-10-01.

Clinical development snapshot

ClinicalTrials.gov lists 122 registered studies with “Colistin” as an intervention (snapshot 2026-10-01). A registry footprint is not evidence of efficacy or approval.

Registered studies
122
Highest phase reached
Phase 4
Active in latest 100
23
Most recent update
2026-09-30
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT06488794Nebulised Colistimethate Sodium to Prevent Pediatric Ventilator-associated PneumoniaPhase 3not yet recruiting2026-09-30
NCT06087536A Clinical Trial to Assess the Safety and PK of OMN6 in HABP or VABP Caused by Acinetobacter Baumannii ComplexPhase 2recruiting2026-09-28
NCT06819462Inhaled Colistin to Prevent Ventilator-Associated Pneumonia in Patients With Acute Brain InjuryNot applicablerecruiting2026-09-15
NCT07512596Study on the Safety and Efficacy of Polymyxin E2 Methanesulfonate for Injection in the Treatment of Hospital-APhase 2recruiting2026-09-04
NCT07082465Epidemiology of Antimicrobial-use and Antimicrobial-resistant Infections in Four Hospitals in Thailand—active not recruiting2026-08-14
NCT07694700Colistin and Meropenem Versus Amikacin and Meropenem for MDR Gram Negative Bacteria Regarding Efficacy and SafPhase 4active not recruiting2026-07-14
See all on ClinicalTrials.gov →
Concentration math

Colistin — reconstitution calculator

Enter how much peptide is in the vial and how much diluent (e.g. bacteriostatic water) is added. The tool returns the resulting solution concentration — and, for any amount you type, the volume it corresponds to. This is educational arithmetic, not a dosing recommendation.

Reference form: Colistin (source record; form not independently established)Average reference mass: 1,155.4 Da

Syringe graduation
Solution concentration
5 mg/mL5,000 mcg/mL
mcg

Enter an amount to see the volume it corresponds to.

Educational concentration mathematics only. This tool does not recommend a dose, amount, or protocol, and nothing here is medical advice. Many peptides are not authorized by Health Canada for human use — see our reconstitution and bacteriostatic-water guides for context.

Open the Colistin calculator on its own page →

FAQ about Colistin

What is Colistin?+

Colistin, also called polymyxin E, is a cyclic lipopeptide antibiotic from Paenibacillus species and a close relative of polymyxin B. It displaces divalent cations from lipopolysaccharide phosphate groups, breaking down the Gram-negative outer membrane. Classified by the WHO as critically important and reserved as a last-resort drug, its usefulness is threatened by the mobile mcr-1 resistance gene. This page is educational and not medical advice.

What Canadian product status is recorded for Colistin?+

Canadian product status for Colistin has not been verified in this profile. No verified record here does not mean no authorization exists. Status depends on the product, formulation and use; consult Health Canada's product records.

What is the typical length of Colistin?+

Colistin 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.El-Sayed Ahmed et al. (2020). Colistin and its role in the Era of antibiotic resistance: an extended review (2000-2019). Emerg Microbes Infect
  2. 2.Krishnakumar et al. (2023). Colistin (Polymyxin E) Use in Abdominal Solid Organ Transplant Recipients. J Pharm Pract
  3. 3.Horton et al. (1982). Polymyxin B, colistin, and sodium colistimethate. Med Clin North Am
  4. 4.Cai et al. (2015). Polymyxin B versus colistin: an update. Expert Rev Anti Infect Ther
  5. 5.Ballı et al. (2024). Battle of polymyxin induced nephrotoxicity: Polymyxin B versus colistin. Int J Antimicrob Agents
  6. 6.Kwa et al. (2007). Polymyxin B: similarities to and differences from colistin (polymyxin E). Expert Rev Anti Infect Ther
  7. 7.Nadeem et al. (2026). Intraventricular colistin for multidrug-resistant ventriculitis: the final therapeutic option?. Neurosurg Rev
  8. 8.Tran et al. (2016). Pharmacokinetics/pharmacodynamics of colistin and polymyxin B: are we there yet?. Int J Antimicrob Agents
  9. 9.PubChem — compound summary for Colistin (CID 5311054)
  10. 10.Wikipedia — Colistin
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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