The components and activities analysis of a novel anticoagulant candidate dHG-5

Eur J Med Chem. 2020 Dec 1:207:112796. doi: 10.1016/j.ejmech.2020.112796. Epub 2020 Sep 6.

Abstract

Intrinsic Xase (iXase), the last and rate-limiting enzyme complex in the intrinsic coagulation pathway, may be an ideal target for antithrombotic treatment. A depolymerized fraction of fucosylated glycosaminoglycan from sea cucumber Holothuria fuscopunctata, dHG-5 (Mw 5.2 kDa), showed potent and selective inhibition of iXase (IC50, 14 nM). In this work, the series of oligosaccharides contained in dHG-5 were purified and their precise structures were confirmed by 2D NMR and MS spectra. The relationships between anti-iXase, f.IXa-binding, anticoagulant and antithrombotic activities (y) and molecular weight (x) could be approximately expressed as the power function (y = a × xb), and these activity potencies of dHG-5 were approximately equivalent to the weighted average sum of that of its oligosaccharides. Given the prominent pharmacological properties, well-defined chemical composition and explicable relationships between dHG-5 and its oligosaccharides in pharmacological behaviors, dHG-5 is expected to be an ideal novel anticoagulant medicine.

Keywords: Anticoagulation; Antithrombosis; FG oligosaccharides; dHG-5; iXase inhibitor.

MeSH terms

  • Animals
  • Anticoagulants / chemistry
  • Anticoagulants / metabolism
  • Anticoagulants / pharmacology*
  • Factor IXa / metabolism
  • Glycosaminoglycans / chemistry
  • Glycosaminoglycans / metabolism
  • Glycosaminoglycans / pharmacology*
  • Inhibitory Concentration 50
  • Molecular Weight
  • Sea Cucumbers / chemistry*

Substances

  • Anticoagulants
  • Glycosaminoglycans
  • Factor IXa