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Neuropeptide

Dynorphin

Dynorphin is a family of endogenous opioid peptides (dynorphin A is 17 residues) derived from prodynorphin. It preferentially activates kappa-opioid receptors and is studied in stress and mood neurobiology.

By The Peptides Codex Editorial TeamIndividual review date not recorded

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

Reference backbone length
17 positions
Class
Neuropeptide
Function
Kappa-opioid signaling and mood/stress modulation
Context
Neuroscience research

Endogenous opioid with high preference for kappa-opioid receptors.

Also known as: Dynorphin A

Part of the Neuropeptides & signaling cluster

Overview

Dynorphin is a family of endogenous opioid peptides (dynorphin A is 17 residues) derived from prodynorphin. It preferentially activates kappa-opioid receptors and is studied in stress and mood neurobiology.

Source & context

Biological / chemical source: Central nervous system; derived from prodynorphin

Primary research or clinical context: Neuroscience research

Kappa-opioid preference

Unlike endorphins, dynorphins act mainly at kappa-opioid receptors and are associated in research with dysphoric and stress-related signaling — a contrast that illustrates how opioid peptide subtypes differ in function.

Prodynorphin family

Prodynorphin is cleaved into several related peptides, including dynorphin A, dynorphin B, and the neoendorphins. This precursor biology is a common theme in opioid-peptide education.

Sequence of the selected reference form

Sequence backbone for the reference form: Human dynorphin A(1-17), defined L stereochemistry and C-terminal free acid. Termini, stereochemistry and modifications are described below.

YGGFLRRIRPKLKWDNQ

YGGFLRRIRPKLKWDNQ

Dynorphin17 aa · C99H155N31O23 · ≈ 2,147.5 Da · Free L-glutamine carboxylic acid (-COOH)PEPTIDESCODEX.COMN-terminus →→ C-terminusY1G2G3F4L5R+6R+7I8R+9P10K+11L12K+13W14D−15N16Q17nonpolarpolaracidicbasicGly / Pronon-canonical (X)Hydropathy (Kyte–Doolittle): ▮ hydrophobic (cyan) / ▮ hydrophilic (rose) · Side-chain charge at pH 7: + / −
Dynorphin — Structure cardDownload SVG
Y1G2G3F4L5R6R7I8R9P10K11L12K13W14D15N16Q17
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

Select human dynorphin A(1-17), not the broader dynorphin family. The reviewed human processed chain and molecular graph agree. Choose the CID with all 16 stereocentres defined rather than the chemically underspecified legacy record.

Molecular form
Human dynorphin A(1-17), defined L stereochemistry and C-terminal free acid
Species
Homo sapiens
Termini (N / C)
Free alpha-amino group of L-tyrosine / Free L-glutamine carboxylic acid (-COOH)

Average reference mass · Molecular identity assessment: 2026-10-05

Reference policy updated: 2026-10-05

Molecular formula
C99H155N31O23
Average reference mass
≈ 2,147.5
Backbone
Human dynorphin A(1-17), defined L stereochemistry and C-terminal free acid
C-terminus
Free L-glutamine carboxylic acid (-COOH)
Identifiers

Chemistry values: curated profile, PubChem.

Clinical development snapshot

ClinicalTrials.gov lists 6 registered studies with “Dynorphin” as an intervention (snapshot 2026-10-01). A registry footprint is not evidence of efficacy or approval.

Registered studies
6
Highest phase reached
Phase 4
Active in latest 100
2
Most recent update
2026-09-23
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT07404358Dalargin for Prevention of Organ Disfunction in High-Risk Abdominal SurgeryPhase 3completed2026-09-23
NCT07139106Understanding the Role of the Kappa Opioid Receptor in Ketamine's Attenuation of Suicidal ThoughtsPhase 4not yet recruiting2026-08-03
NCT07583160YS247 (Neoantigen-Pulsed DC Vaccine) for Metastatic Prostate CancerPhase 1enrolling by invitation2026-05-13
NCT04108546Massage and Electroacupuncture in Chronic Lumbar PainNot applicablecompleted2025-03-28
NCT00000244Effects of Dynorphin 1-13 on Heroin Addiction - 1Phase 2completed2015-05-27
NCT02092805rTMS as a Treatment of Visceral Pain Secondary to MalignancyNot applicablecompleted2014-03-20
See all on ClinicalTrials.gov →
Concentration math

Dynorphin — 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: Human dynorphin A(1-17), defined L stereochemistry and C-terminal free acidAverage reference mass: 2,147.5 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 Dynorphin calculator on its own page →

FAQ about Dynorphin

What is Dynorphin?+

Dynorphin is a family of endogenous opioid peptides (dynorphin A is 17 residues) derived from prodynorphin. It preferentially activates kappa-opioid receptors and is studied in stress and mood neurobiology.

What Canadian product status is recorded for Dynorphin?+

Canadian product status for Dynorphin 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 length of the selected reference form for Dynorphin?+

The selected reference form (Human dynorphin A(1-17), defined L stereochemistry and C-terminal free acid) has 17 residues or residue-derived units in its backbone. Other forms in this family may have a different length.

Related peptides

References & further reading

  1. 1.Vanderah et al. (1996). Single intrathecal injections of dynorphin A or des-Tyr-dynorphins produce long-lasting allodynia in rats: blockade by MK-801 but not naloxone. Pain
  2. 2.Dai et al. (2025). Dynorphin A Impairs Mitochondrial Biogenesis in Osteosarcoma Cells by Increasing SP-1. J Biochem Mol Toxicol
  3. 3.Hall et al. (2016). Dynorphin A analogs for the treatment of chronic neuropathic pain. Future Med Chem
  4. 4.Brugos et al. (2004). Metabolism of dynorphin A(1-13). Pharmazie
  5. 5.Lee et al. (2016). Cyclic non-opioid dynorphin A analogues for the bradykinin receptors. Bioorg Med Chem Lett
  6. 6.Marinelli et al. (2006). A microdialysis profile of dynorphin A(1-8) release in the rat nucleus accumbens following alcohol administration. Alcohol Clin Exp Res
  7. 7.LaVigne et al. (2023). Pain-related behavioral and electrophysiological actions of dynorphin A (1-17). Mol Pain
  8. 8.Friedman et al. (1981). Dynorphin: a possible modulatory peptide on morphine or beta-endorphin analgesia in mouse. Eur J Pharmacol
  9. 9.PubChem — compound summary for Dynorphin A (CID 16129685)
  10. 10.Wikipedia — Dynorphin
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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