Marine Drugs · 2019 · 16 citations · 34 references
MedicineBiochemistryPharmacologyBiochemical PharmacologyGlycobiologyHemostasisAnticoagulant TherapyFibrin FormationGlycan AnalysisGlycan StructureGlycan-protein InteractionsNatural Anticoagulant SystemsGlycosaminoglycansHeparin-mediated AnticoagulationHeparin-protein InteractionsPlasma Anticoagulant ActivityProthrombin ActivationThrombin Time
, which shows potent anticoagulant and fibrinolytic abilities. Its structure was characterized by infrared spectroscopy, high-performance liquid chromatography, and one-dimensional and two-dimensional nuclear magnetic resonance spectroscopy. Its fibrinolytic activity was determined in vitro and in vivo. Its anticoagulant activity was determined by activated partial thromboplastin time (APTT), prothrombin time (PT), and thrombin time (TT). The results indicated that clam heparinoid was a homogeneous glycosaminoglycan with a molecular weight of 30.99 kDa, mainly composed of →4)-α-IdoA2S-(1→4)-α-GlcNS3S6S (or GlcNS6S)-(1→4)-β-GlcA-(1→4)-α-GlcNS6S (or GlcNAC)-(1→. Furthermore, this heparinoid showed a highly anticoagulant titer and fibrinolytic value of 149.63 IU/mg and 1.96 IU/mg, respectively. In summary, clam heparinoid shows great potential for application in the clinic and antithrombotic drugs industry.
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