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Signaling peptide (kinin)

Bradykinin

Bradykinin is a nine-amino-acid signaling peptide of the kinin group, released from kininogen by kallikrein.

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
9 aa
Class
Signaling peptide (kinin)
Function
Vasodilator and inflammatory mediator via bradykinin B2/B1 receptors
Context
Vascular, inflammation and pain physiology research

A nine-residue kinin that dilates vessels, raises permeability and signals pain during inflammation.

Also known as: BK · kallidin-related kinin

Part of the Foundational & therapeutic peptides cluster

Overview

Bradykinin is a nine-amino-acid signaling peptide of the kinin group, released from kininogen by kallikrein. Acting through B2 and B1 receptors, it drives vasodilation, increased vascular permeability, pain signaling and inflammation, and is central to the kallikrein-kinin system. This page is educational and not medical advice.

Source & context

Biological / chemical source: Cleaved from kininogen by kallikrein enzymes

Primary research or clinical context: Vascular, inflammation and pain physiology research

Generation and receptors

Bradykinin (RPPGFSPFR) is cleaved from high-molecular-weight kininogen by plasma kallikrein. It acts mainly at the constitutive B2 receptor and, during injury, at the inducible B1 receptor, and is rapidly degraded by kininases including angiotensin-converting enzyme (ACE).

Why it matters

Because ACE also inactivates bradykinin, its accumulation explains the cough and angioedema seen with ACE-inhibitor drugs. The peptide is a key research model for vascular permeability, nociception and hereditary angioedema, where kallikrein-kinin signaling is dysregulated.

Sequence

One-letter sequence commonly cited for Bradykinin (educational; isoforms and modifications may differ):

RPPGFSPFR

RPPGFSPFR

Bradykinin9 aa · C50H73N15O11 · ≈ 1,060.2 DaPEPTIDESCODEX.COMN-terminus →→ C-terminusR+1P2P3G4F5S6P7F8R+9nonpolarpolaracidicbasicGly / Pronon-canonical (X)Hydropathy (Kyte–Doolittle): ▮ hydrophobic (cyan) / ▮ hydrophilic (rose) · Side-chain charge at pH 7: + / −
Bradykinin — Structure cardDownload SVG
R1P2P3G4F5S6P7F8R9
Helical wheel projection

Residues plotted ~100° apart around an α-helix — clustering of one color reveals an amphipathic face.

Analyze sequences in the playground →

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
Bradykinin (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
C50H73N15O11
Average reference mass
≈ 1,060.2
Identifiers

Chemistry values: PubChem, IUPHAR/BPS Guide to Pharmacology · fetched 2026-09-06.

Clinical development snapshot

ClinicalTrials.gov lists 73 registered studies with “Bradykinin” as an intervention (snapshot 2026-10-01). A registry footprint is not evidence of efficacy or approval.

Registered studies
73
Highest phase reached
Phase 4
Active in latest 100
12
Most recent update
2026-09-22
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT06679881Long-Term, Open-label Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema APhase 3enrolling by invitation2026-09-22
NCT07266805Study of Oral Deucrictibant XR Tablet for Prophylaxis and Deucrictibant Soft Capsule for On-Demand Treatment oPhase 3recruiting2026-09-21
NCT07800338Evaluation Of The Effect Of Low-Level Laser Therapy On Masseter Muscle Versus Therapeutic Ultrasound On PatienNot applicablenot yet recruiting2026-09-02
NCT05630612ETA and AT1 Antagonism in ANCA-vasculitis (SPARVASC)Phase 2active not recruiting2026-08-26
NCT05047185Dose-ranging Study of Oral PHA-022121 for Prophylaxis Against Angioedema Attacks in Patients With Hereditary APhase 2terminated2026-08-17
NCT07759141EAP for Deucrictibant Immediate-release—available2026-08-12
See all on ClinicalTrials.gov →
Concentration math

Bradykinin — 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: Bradykinin (source record; form not independently established)Average reference mass: 1,060.2 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 Bradykinin calculator on its own page →

FAQ about Bradykinin

What is Bradykinin?+

Bradykinin is a nine-amino-acid signaling peptide of the kinin group, released from kininogen by kallikrein. Acting through B2 and B1 receptors, it drives vasodilation, increased vascular permeability, pain signaling and inflammation, and is central to the kallikrein-kinin system. This page is educational and not medical advice.

What Canadian product status is recorded for Bradykinin?+

Canadian product status for Bradykinin 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 Bradykinin?+

Bradykinin is commonly described as approximately 9 amino acids (Signaling peptide (kinin)).

Related peptides

References & further reading

  1. 1.Lepinski et al. (2000). Bradykinin levels in dental pulp by microdialysis. J Endod
  2. 2.Sachs et al. (2018). [Drug-induced angioedema : Focus on bradykinin]. Hautarzt
  3. 3.Takano et al. (2014). Intracellular and nuclear bradykinin B2 receptors. Eur J Pharmacol
  4. 4.Yin et al. (2021). Molecular basis for kinin selectivity and activation of the human bradykinin receptors. Nat Struct Mol Biol
  5. 5.Yi et al. (2024). Bradykinin receptor expression and bradykinin-mediated sensitization of human sensory neurons. Pain
  6. 6.Song et al. (2024). Bradykinin attenuates endothelial-mesenchymal transition following cardiac ischemia-reperfusion injury. Eur J Pharmacol
  7. 7.Francel (1992). Bradykinin and neuronal injury. J Neurotrauma
  8. 8.Siti-Zubaidah et al. (2024). Exploring bradykinin: A common mediator in the pathophysiology of sepsis and atherosclerotic cardiovascular disease. Vascul Pharmacol
  9. 9.PubChem — Bradykinin (CID 439201)
  10. 10.Wikipedia — Bradykinin
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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