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GPIIb/IIIa inhibitor

Eptifibatide

Eptifibatide is a synthetic cyclic heptapeptide derived from a disintegrin in pygmy rattlesnake venom.

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
7 aa
Class
GPIIb/IIIa inhibitor
Function
Glycoprotein IIb/IIIa receptor antagonist (antiplatelet)
Context
Approved for acute coronary syndrome and percutaneous coronary intervention

A venom-derived cyclic heptapeptide that blocks platelet aggregation.

Also known as: Integrilin

Part of the Foundational & therapeutic peptides cluster

Overview

Eptifibatide is a synthetic cyclic heptapeptide derived from a disintegrin in pygmy rattlesnake venom. It reversibly blocks the platelet glycoprotein IIb/IIIa receptor, the final common step of platelet aggregation, and it is an approved antiplatelet therapeutic for acute coronary syndrome and coronary intervention. Content here is educational only.

Source & context

Biological / chemical source: Synthetic cyclic heptapeptide from snake-venom disintegrin

Primary research or clinical context: Approved for acute coronary syndrome and percutaneous coronary intervention

Disintegrin mimicry

Snake-venom disintegrins interrupt clotting by mimicking the RGD/KGD motif that binds platelet integrins. Eptifibatide captures this KGD-mimetic motif in a stable cyclic peptide, a well-known example of venom-inspired drug design.

Final-step blockade

Because glycoprotein IIb/IIIa engagement with fibrinogen is the last step in platelet cross-linking, blocking it prevents aggregation regardless of the activating stimulus. Its reversible binding is often contrasted with irreversible antiplatelet agents in cardiology teaching.

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
Eptifibatide (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
C35H49N11O9S2
Average reference mass
≈ 832
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 35 registered studies with “Eptifibatide” as an intervention (snapshot 2026-09-06). A registry footprint is not evidence of efficacy or approval.

Registered studies
35
Highest phase reached
Phase 4
Active in latest 100
1
Most recent update
2026-01-16
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT07347626Eptifibatide for Extended Window Ischemic Stroke After ThrombolysisPhase 3not yet recruiting2026-01-16
NCT03735979Multi-arm Optimization of Stroke ThrombolysisPhase 3completed2025-02-07
NCT00089895EARLY ACS: Early Glycoprotein IIb/IIIa Inhibition in Patients With Non-ST-segment Elevation Acute Coronary SynPhase 3completed2024-05-17
NCT05415150Platelet Function in Patients With Ischemic Stroke Treated With Anti-thrombotic or ThrombolyticPhase 2unknown2022-06-10
NCT01991366Should Integrilin be an Integral Part of Adjunctive Therapy in Patients Undergoing Primary PCI for ST-Elevatio—withdrawn2021-07-02
NCT01522417Shortened Aggrastat® Versus Integrilin in Percutaneous Coronary InterventionPhase 2completed2021-05-13
See all on ClinicalTrials.gov →
Concentration math

Eptifibatide — 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: Eptifibatide (source record; form not independently established)Average reference mass: 832 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 Eptifibatide calculator on its own page →

FAQ about Eptifibatide

What is Eptifibatide?+

Eptifibatide is a synthetic cyclic heptapeptide derived from a disintegrin in pygmy rattlesnake venom. It reversibly blocks the platelet glycoprotein IIb/IIIa receptor, the final common step of platelet aggregation, and it is an approved antiplatelet therapeutic for acute coronary syndrome and coronary intervention. Content here is educational only.

What Canadian product status is recorded for Eptifibatide?+

Canadian product status for Eptifibatide 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 Eptifibatide?+

Eptifibatide is commonly described as approximately 7 amino acids (GPIIb/IIIa inhibitor).

Related peptides

References & further reading

  1. 1.Adeoye et al. (2024). Adjunctive Intravenous Argatroban or Eptifibatide for Ischemic Stroke. N Engl J Med
  2. 2.Roy et al. (2025). Thrombolysis Alone vs With Argatroban or Eptifibatide: A Prespecified Subgroup Analysis of the MOST Trial. Neurology
  3. 3.Rines et al. (2025). Intravenous Argatroban or Eptifibatide in Patients Undergoing Mechanical Thrombectomy: A Subgroup Analysis of the MOST Randomized Clinical Trial. JAMA Neurol
  4. 4.Waldron et al. (2017). Bleeding risk associated with eptifibatide (Integrilin) bridging in thoracic surgery patients. J Thromb Thrombolysis
  5. 5.Parakh et al. (2009). Eptifibatide overdose. Int J Cardiol
  6. 6.Phillips et al. (1997). Clinical pharmacology of eptifibatide. Am J Cardiol
  7. 7.Scarborough (1999). Development of eptifibatide. Am Heart J
  8. 8.Holmvang et al. (2001). [Eptifibatide (Integrilin)]. Ugeskr Laeger
  9. 9.PubChem — compound summary for Eptifibatide (CID 448812)
  10. 10.Wikipedia — Eptifibatide
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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