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Bivalirudin TFA

Cat. No. M14537

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Bivalirudin TFA Structure
Size Price Availability Quantity
5mg USD 45 In stock
10mg USD 70 In stock
50mg USD 120 In stock
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Quality Control & Documentation
Biological Activity

Bivalirudin TFA is a synthetic 20 residue peptide which reversibly inhibits thrombin. IC50 Value: Target: thrombin in vitro: Eptifibatide (8 mg/mL) added together with a low (70 ng/mL) concentration of bivalirudin (a direct thrombin inhibitor) effectively (approximately 90%) reduced platelet aggregation induced by thrombin (0.2 U/mL). In thrombin generation assay (TGA), bivalirudin had no effect on these parameters up to 10 μmol/l. Bivalirudin-facilitated binding of MPO to BAEC resulted also in functional changes in terms of increased NO consumption as well as enhanced MPO-mediated redox modifications. in vivo: The use of bivalirudinprevented further increase in antiheparin/PF4 antibody IgG levels in rats. Three animals in the 500-mg/kg/24 h group, and 7 animals in the 2000-mg/kg/24 h group in the toxicokinetic assessment phase of the study were found dead or euthanized in extremis (following blood sampling). Plasma concentrations of bivalirudin appeared to be linear and dose independent. Clinical trial: Antithrombotic Effects of Ticagrelor Versus Clopidogrel . Phase 4

Chemical Information
Molecular Weight 2294.34
CAS Number 1191386-55-6
Solubility (25°C) Water 90 mg/mL
DMSO ≥ 31 mg/mL
Storage -20°C, protect from light, dry, sealed
References

[1] Yuying Huang, et al. Thrombin cleaves IL-33 and modulates IL-33-activated allergic lung inflammation

[2] Don Farthing, et al. Liquid chromatography method for determination of bivalirudin in human plasma and urine using automated ortho-phthalaldehyde derivatization and fluorescence detection

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Keywords: Bivalirudin TFA supplier, Thrombopoietin/Thrombin, inhibitors, activators

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