Sociedad Americana de Hirudoterapia

Phospho-Hirudin (pY63 variant)

Synthetic phosphotyrosine-63 hirudin analog with higher thrombin affinity than native sulfo-hirudin — Volkova 2023 steered-MD + in vitro plasma assay.

Preclínico / mecanísticoLast updated: 2026-05-27 · Reviewed by ASH Editorial Board
Molecular weight of Phospho-Hirudin (pY63 variant) 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 kDaPhospho-Hirudin (pY63 variant)7 kDa
Molecular weight (kilodaltons) of Phospho-Hirudin (pY63 variant) (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
Synthetic phosphotyrosine-63 hirudin analog with higher thrombin affinity than native sulfo-hirudin — Volkova 2023 steered-MD + in vitro plasma assay.
Evidence level
In vitro
Drug vs leech
Synthetic analog
Safety domains
Bleeding

Clinical translation limit

Phospho-hirudin's superior in silico binding and in vitro plasma activity do NOT establish clinical efficacy. No FDA-approved phospho-hirudin derivative exists; clinical hirudin analogs (lepirudin, desirudin, bivalirudin) use different post-translational modifications.

Molecular Profile

Category
Anticoagulant
Evidence tier
Preclinical
Molecular weight
7,000 Da
Source species
Hirudo medicinalis (sequence template)
Discovered
2023 · Volkova A, Semenyuk P
Phospho-Hirudin (pY63 variant) molecular structure

Biological Targets

  • thrombin (Factor IIa); Tyr63 phosphate enhances binding to exosite I

Key Citations

  1. Volkova A, Semenyuk P (2023), Proteins · PMID 37860993

External Resources

    Related Anticoagulant Compounds

    Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.