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Conotoxin analgesic

Ziconotide

Ziconotide is the synthetic form of an ω-conotoxin, a 25-amino-acid peptide from cone snail venom that selectively blocks N-type voltage-gated calcium channels.

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
25 aa
Class
Conotoxin analgesic
Function
N-type voltage-gated calcium channel blocker
Context
Approved for severe chronic pain via intrathecal infusion

A cone-snail venom peptide that blocks N-type calcium channels for pain.

Also known as: Prialt

Part of the Foundational & therapeutic peptides cluster

Overview

Ziconotide is the synthetic form of an ω-conotoxin, a 25-amino-acid peptide from cone snail venom that selectively blocks N-type voltage-gated calcium channels. Delivered directly into cerebrospinal fluid by an intrathecal pump, it is an approved therapeutic for severe, refractory chronic pain. Content here is educational only.

Source & context

Biological / chemical source: Synthetic ω-conotoxin from cone snail venom

Primary research or clinical context: Approved for severe chronic pain via intrathecal infusion

Venom to medicine

Cone snails paralyze prey with peptide toxins, and ω-conotoxin's precise blockade of N-type calcium channels interrupts pain-signal transmission in the spinal cord. Ziconotide is a landmark example of a marine venom peptide developed into an approved drug.

Intrathecal delivery

Because the peptide does not cross the blood-brain barrier, it must be infused into the cerebrospinal fluid through an implanted pump. This delivery constraint is often used to teach how a peptide's physical properties dictate its route of administration.

Sequence

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

CKGKGAKCSRLMYDCCTGSCRSGKC

CKGKGAKCSRLMYDCCTGSCRSGKC

Ziconotide25 aa · C102H172N36O32S7 · ≈ 2,639.2 DaPEPTIDESCODEX.COMN-terminus →→ C-terminusC1K+2G3K+4G5A6K+7C8S9R+10L11M12Y13D−14C15C16T17G18S19C20R+21S22G23K+24C25nonpolarpolaracidicbasicGly / Pronon-canonical (X)Hydropathy (Kyte–Doolittle): ▮ hydrophobic (cyan) / ▮ hydrophilic (rose) · Side-chain charge at pH 7: + / −
Ziconotide — Structure cardDownload SVG
C1K2G3K4G5A6K7C8S9R10L11M12Y13D14C15C16T17G18S19C20R21S22G23K24C25
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
Ziconotide (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
C102H172N36O32S7
Average reference mass
≈ 2,639.2
Status
Approved medicine in at least one jurisdiction (IUPHAR record)
Identifiers

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

Clinical development snapshot

ClinicalTrials.gov lists 14 registered studies with “Ziconotide” as an intervention (snapshot 2026-10-01). A registry footprint is not evidence of efficacy or approval.

Registered studies
14
Highest phase reached
Phase 4
Active in latest 100
4
Most recent update
2026-09-10
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT07733427Evaluating the Effectiveness of AIT in the Treatment of Pain Related to Pancreatic CancerNot applicablenot yet recruiting2026-09-10
NCT07499882Intrathecal Ziconotide in Chemotherapy Induced Peripheral Neuropathy—not yet recruiting2026-03-30
NCT04321408OP2C : Prialt® Observatory in Clinical Practice—recruiting2025-08-17
NCT06541184Ziconotide for Non-cancer Pain by Intrathecal Administration—recruiting2025-02-27
NCT00996983Safety and Activity Study of Intrathecally Administered Ziconotide for Neuropathic Pain in Patients With CancePhase 2unknown2023-03-24
NCT03321955Ziconotide as First-Line IDTPhase 4completed2021-01-12
See all on ClinicalTrials.gov →
Concentration math

Ziconotide — 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: Ziconotide (source record; form not independently established)Average reference mass: 2,639.2 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 Ziconotide calculator on its own page →

FAQ about Ziconotide

What is Ziconotide?+

Ziconotide is the synthetic form of an ω-conotoxin, a 25-amino-acid peptide from cone snail venom that selectively blocks N-type voltage-gated calcium channels. Delivered directly into cerebrospinal fluid by an intrathecal pump, it is an approved therapeutic for severe, refractory chronic pain. Content here is educational only.

What Canadian product status is recorded for Ziconotide?+

Canadian product status for Ziconotide 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 Ziconotide?+

Ziconotide is commonly described as approximately 25 amino acids (Conotoxin analgesic).

Related peptides

References & further reading

  1. 1.Lyseng-Williamson et al. (2006). Ziconotide. CNS Drugs
  2. 2.Strigenz (2014). Ziconotide. J Pain Palliat Care Pharmacother
  3. 3.Fisher et al. (2005). A consensus statement regarding the present suggested titration for prialt (ziconotide). Neuromodulation
  4. 4.Lynch et al. (2006). Intrathecal ziconotide for refractory chronic pain. Ann Pharmacother
  5. 5.Lin et al. (2024). A comprehensive review on ziconotide. Heliyon
  6. 6.Rubiu et al. (2024). A Benefit/Risk Assessment of Intrathecal Ziconotide in Chronic Pain: A Narrative Review. J Clin Med
  7. 7.Sanford (2013). Intrathecal ziconotide: a review of its use in patients with chronic pain refractory to other systemic or intrathecal analgesics. CNS Drugs
  8. 8.Rauck et al. (2009). Intrathecal ziconotide for neuropathic pain: a review. Pain Pract
  9. 9.PubChem — compound summary for Ziconotide (CID 16135415)
  10. 10.Wikipedia — Ziconotide
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 — Ziconotide educational profile.
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