Sociedad Americana de Hirudoterapia

Leech Nitric Oxide Synthase Modulator

Modulates host NOS activity at bite site — contributes to vasodilation phase of feeding.

Preclínico / mecanísticoLast updated: 2026-05-26 · Reviewed by ASH Editorial Board
Molecular weight of Leech Nitric Oxide Synthase Modulator 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 Nitric Oxide Synthase M…22 kDa
Molecular weight (kilodaltons) of Leech Nitric Oxide Synthase Modulator (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
Modulates host NOS activity at bite site — contributes to vasodilation phase of feeding.
Evidence level
Mechanistic discussion
Drug vs leech
Leech-derived crude extract

Clinical translation limit

The vasodilatory role of leech NOS modulation at the bite site is mechanistic only and does not establish clinical efficacy for any vasodilation-related indication. No FDA-approved derivative exists.

Molecular Profile

Category
Vasodilator
Evidence tier
Preclinical
Molecular weight
22,000 Da
Source species
Hirudo medicinalis
Leech Nitric Oxide Synthase Modulator molecular structure

Biological Targets

  • nitric oxide synthase (NOS) pathway

External Resources

    Related Vasodilator Compounds

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