Sociedad Americana de Hirudoterapia

Leech Kallikrein Inhibitor

Plasma kallikrein-kinin system modulator — anti-inflammatory pathway distinct from cyclooxygenase.

Preclínico / mecanísticoLast updated: 2026-05-26 · Reviewed by ASH Editorial Board
Molecular weight of Leech Kallikrein Inhibitor 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 kDaLeech Kallikrein Inhibitor7.5 kDa
Molecular weight (kilodaltons) of Leech Kallikrein Inhibitor (highlighted) alongside other characterized leech salivary compounds. Smaller proteins/peptides generally diffuse and act faster.

Mechanistic Evidence Box

Preclinical / mechanistic
Page type
Compound profile
Evidence type
Plasma kallikrein-kinin system modulator — anti-inflammatory pathway distinct from cyclooxygenase.
Evidence level
Mechanistic discussion
Drug vs leech
Purified natural compound

Clinical translation limit

Leech kallikrein inhibitor's mechanism is preclinical only. No FDA-approved derivative exists; not to be confused with the FDA-approved synthetic kallikrein inhibitor ecallantide (Kalbitor), which is a separate pharmaceutical product.

Molecular Profile

Category
Proteinase Inhibitor
Evidence tier
Preclinical
Molecular weight
7,500 Da
Source species
Hirudo medicinalis
Leech Kallikrein Inhibitor molecular structure

Biological Targets

  • plasma kallikrein

External Resources

    Related Proteinase Inhibitor Compounds

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