Skip to content

Ziconotide

N-type Calcium Channel Antagonist — NERVOUS SYSTEM

Also known as: omega-Conopeptide MVIIA (Conus), prialt, ziconotide acetate

FDA approvedATC N02BG08

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Ziconotide is a drug in the N-type Calcium Channel Antagonist class catalogued in DrugCentral. It was first approved by the FDA in 2004. Its mechanism of action is classified as N-Calcium Channel Receptor Antagonists. DrugCentral lists 3 molecular targets, including Cacna1b, Cacna1a and CACNA1B. Recorded indications include Chronic pain, Chronic Pain with Opioid Tolerance, Pain in spine and Severe pain.

  • Drug class: N-type Calcium Channel Antagonist.
  • Mechanism of action: N-Calcium Channel Receptor Antagonists.
  • Molecular targets: Cacna1b, Cacna1a and CACNA1B (3 listed in DrugCentral).
  • Indications: Chronic pain, Chronic Pain with Opioid Tolerance, Pain in spine and Severe pain.
  • ATC code: N02BG08 (Other analgesics and antipyretics).
  • Molecular formula: C102H172N36O32S7; molecular weight 2639.14 g/mol.

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (4)

  • Chronic pain
  • Chronic Pain with Opioid Tolerance
  • Pain in spine
  • Severe pain

Contraindications (3)

  • Blood coagulation disorder
  • Increased Creatine Phosphokinase
  • Psychotic disorder

Mechanism & targets

Mechanism of action (MoA)N-Calcium Channel Receptor Antagonists
Established pharmacologic classN-type Calcium Channel Antagonist

Molecular targets (3)

TargetGeneActionActivity
Voltage-dependent N-type calcium channel subunit alpha-1BCacna1bblockerIC50 10.30
Voltage-dependent P/Q-type calcium channel subunit alpha-1ACacna1ablockerIC50 6.30
Voltage-dependent N-type calcium channel subunit alpha-1BCACNA1Bblocker—

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
2004-12-28FDA—JAZZ PHARMS INTL

ATC classification

ATC codeTherapeutic hierarchy
N02BG08NERVOUS SYSTEM › ANALGESICS › OTHER ANALGESICS AND ANTIPYRETICS › Other analgesics and antipyretics

Reported adverse-event signals

Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.

MedDRA termLLR
Device issue289.1
Hallucination, auditory193.3
Hallucination167.8
Confusional state166.0
Drug withdrawal syndrome100.7
Mental status changes93.9
Psychotic disorder68.3
Hallucination, visual59.7
Nystagmus51.6
Withdrawal syndrome50.8
Urinary retention46.3
Burning sensation42.6

Chemical structure

Molecular formulaC102H172N36O32S7
Molecular weight2639.14 g/mol
CAS number107452-89-1
InChIKeyBPKIMPVREBSLAJ-QTBYCLKRSA-N
PubChem CID16135415
CSCC[C@@H]1NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@@H]2CSSC[C@@H]3NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](CSSC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N2)NC(=O)[C@H](CSSC[C@H](NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CCCNC(N)=N)NC3=O)C(N)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC2=CC=C(O)C=C2)NC1=O)[C@@H](C)O

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Ziconotide used for?

DrugCentral lists the following indications for Ziconotide: Chronic pain, Chronic Pain with Opioid Tolerance, Pain in spine and Severe pain.

How does Ziconotide work?

Ziconotide is classified as N-Calcium Channel Receptor Antagonists; its molecular targets in DrugCentral include Cacna1b (blocker), Cacna1a (blocker) and CACNA1B (blocker).

When was Ziconotide first approved?

Ziconotide was first approved by the FDA in 2004.

What drug class does Ziconotide belong to?

Ziconotide is in the N-type Calcium Channel Antagonist class.

What is the chemical formula of Ziconotide?

Ziconotide has the molecular formula C102H172N36O32S7 and a molecular weight of 2639.14 g/mol.

Browse: all drugs starting with Z · drug guides by category · protein targets A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

Status—
First approval2004-12-28
AgencyFDA
Targets3
Indications4
FormulaC102H172N36O32S7
DrugCentral ID2878
Interactive profile