Bivalirudin Trifluoroacetate

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Product
Bivalirudin Trifluoroacetate
Posting date : Jun 01, 2015
Membership
Free Member Scince Jun 01, 2015
FOB Price
15 USD
Min. Order Quantity
10g
Supply Abillity
1 ton per month
Port
China
Payment Terms
Western union,Money Gram
Package
Disguised package
Keyword :
Category
Contact
David Lu
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Product Detail
Company Info
 
Quick Detail
Place of Origin
China [CN]
Brand Name
Yuancheng
Model Number
cx05@yccreate.com
HS-CODE
30-
Package & Delivery Lead Time
Package
Disguised package
Delivery Lead Time
within 3 working days
Detailed Description
Detailed Product Description
 
 
98% Injectable Polypeptide Hormones Bivalirudin Trifluoroacetate CAS 128270-60-0 Bivalirudin For Inhibiting Thrombin-mediated Platelet Activation & Aggregation
 
                                              
Quick Details:
 
  • Bivalirudin Trifluoroacetate
  • Sequence:D-Phe-Pro-Arg-Pro-Gly-Gly-Gly-Gly-Asn-Gly-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-OH
  • Alias:126:PN:WO2004076484PAGE:31 claimed protein;Angiomax;BG 8967;Bivalirudin;Hirulog; Hirulog 1
  • Cas No.: 128270-60-0
  • Molecular Formula: C98H138N24O33
  • Molecular Weight: 2180.29
  • Purity (HPLC): 98.0%min.
  • Appearance: White Powder
  • Single Impurity (HPLC): 1.0%max
  • Amino Acid Composition: ±10% of theoretical
  • Peptide Content (N%): >80.0%
  • Water Content (Karl Fischer): <8.0%
  • TrifluoroAcetate Content(HPIC): >12.0%
  • MS (ESI): Consistent
  • Mass Balance: 95.0~105.0%
  • Grade : Pharmaceutical Grade
  • Storage: Closed, below 2 ~ 8℃ preservation
  • Manufacturer :Hezhong
  • Usage : This product is mainly used for the prevention of vascular forming interventional therapy in the treatment of unstable angina, ischemic complications before and after.It inhibits both circulating and clot-bound thrombin, while also inhibiting thrombin-mediated platelet activation and aggregation.
 
Description:
 
Bivalirudin (Angiomax or Angiox, manufactured by The Medicines Company) is a specific and reversible direct thrombin inhibitor (DTI).
Bivalirudin is a DTI that overcomes many limitations seen with indirect thrombin inhibitors, such as heparin. Bivalirudin is a short, synthetic peptide that is potent, highly specific, and a reversible inhibitor of thrombin. It inhibits both circulating and clot-bound thrombin, while also inhibiting thrombin-mediated platelet activation and aggregation. Bivalirudin has a quick onset of action and a short half-life. It does not bind to plasma proteins (other than thrombin) or to red blood cells. Therefore it has a predictable antithrombotic response. There is no risk for Heparin Induced Thrombocytopenia/Heparin Induced Thrombosis-Thrombocytopenia Syndrome (HIT/HITTS). It does not require a binding cofactor such as antithrombin and does not activate platelets. These characteristics make bivalirudin an ideal alternative to heparin.
Bivalirudin clinical studies demonstrated consistent positive outcomes in patients with stable angina, unstable angina (UA), non-ST segment elevation myocardial infarction (NSTEMI), and ST-segment elevation myocardial infarction (STEMI) undergoing PCI in 7 major randomized trials
 
Application:
 
Bivalirudin is indicated for use as an anticoagulant in patients with unstable angina undergoing percutaneous transluminal coronary angioplasty (PTCA).
Bivalirudin with provisional use of glycoprotein IIb/IIIa inhibitor (GPI) is indicated for use as an anticoagulant in patients undergoing percutaneous coronary intervention (PCI).
Bivalirudin is indicated for patients with, or at risk of HIT/HITTS undergoing PCI.
Bivalirudin is intended for use with aspirin and has been studied only in patients receiving concomitant aspirin.
 
Specifications :
 
Product name
Bivalirudin Trifluoroacetate
Appearance
White Powder
Assay
98%min
Molecular formula
C98H138N24O33
Molecular weight
2180.29
Package
2mg/vial or as your request
Shipping
Fast and secure shipping by DHL,EMS,UPS,TNT, FedEx..
Shipping leading time
Within 12 hours after receiving the payment
Payment Terms
Western Union, Money Gram , T/T, PayPal
Price
Negotiable
 

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