American Society of Hirudotherapy

Eptifibatide

Cyclic heptapeptide GP IIb/IIIa receptor antagonist — FDA approved 1998. Structural inspiration: leech decorsin.

Studied off-labelLast updated: 2026-05-26 · Reviewed by ASH Editorial Board
Molecular weight of Eptifibatide compared with other characterized leech-derived compoundsHementerin80 kDaHementin80 kDaHementin-Like Protein (HLP-1)80 kDaLeech Collagenase70 kDaHaemadipsa yanyuanensis Progr…70 kDaLeech Apyrase67 kDaCalin65 kDaHyaluronidase60 kDaAntithrombin III binding prot…58 kDaCollagenolytic Fibrinolysin55 kDaLeech Thrombospondin-Like Pro…50 kDaEptifibatide0.8 kDa
Molecular weight (kilodaltons) of Eptifibatide (highlighted) alongside other characterized leech salivary compounds. Smaller proteins/peptides generally diffuse and act faster.

Mechanistic Evidence Box

Studied off-label
Page type
Compound profile
Evidence type
Cyclic heptapeptide GP IIb/IIIa receptor antagonist — FDA approved 1998. Structural inspiration: leech decorsin.
Evidence level
FDA-cleared regulatory context
Drug vs leech
Synthetic analog
Safety domains
Bleeding

Clinical translation limit

Eptifibatide is a synthetic peptidomimetic drug whose design drew on both snake venom (Sistrurus) and leech decorsin disintegrin scaffolds; it is chemically distinct from both. Its RCT evidence base (EPISTENT) applies only to the drug, not to whole medicinal-leech therapy.

Molecular Profile

Category
Antiplatelet
Evidence tier
Tier A — FDA-approved derivative
Molecular weight
831.96 Da
Source species
Synthetic peptidomimetic
Discovered
1993 · COR Therapeutics / Millennium Pharmaceuticals (originally inspired by Sistrurus snake venom + leech decorsin)
PubChem CID
123610
Derived FDA-approved drug
Integrilin (FDA approved May 1998)
Eptifibatide molecular structure

Biological Targets

  • platelet integrin αIIbβ3 (GP IIb/IIIa)

Key Citations

  1. PURSUIT Trial Investigators (1998), N Engl J Med · PMID 9705684

Related Antiplatelet Compounds

This website provides educational information and does not constitute medical advice, diagnosis, or treatment recommendations. Medicinal leech therapy carries clinically meaningful risks and should be performed only by qualified clinicians under institutionally approved protocols. FDA 510(k) clearance for medicinal leeches is limited to specific indications; investigational and off-label discussions are labeled accordingly. For patient-specific guidance, consult a qualified healthcare provider.