CAS 128270-60-0
:Bivalirudin
Description:
Bivalirudin is a synthetic peptide that functions as a direct thrombin inhibitor, primarily used as an anticoagulant in clinical settings, particularly during percutaneous coronary interventions. Its structure consists of 20 amino acids, and it is derived from the hirudin peptide found in leeches. Bivalirudin exhibits a high affinity for thrombin, effectively preventing the conversion of fibrinogen to fibrin, which is crucial in the clotting process. The substance is administered via intravenous injection and has a relatively short half-life, necessitating careful monitoring of anticoagulation levels during treatment. Bivalirudin is characterized by its stability in the bloodstream and its ability to provide rapid anticoagulation with a predictable pharmacokinetic profile. It is often favored over traditional anticoagulants due to its lower risk of inducing thrombocytopenia and its ease of use in patients with varying renal function. Overall, Bivalirudin represents a significant advancement in anticoagulant therapy, particularly in acute coronary syndrome management.
Formula:C98H138N24O33
InChI:InChI=1/C98H138N24O33/c1-5-52(4)82(96(153)122-39-15-23-70(122)92(149)114-60(30-34-79(134)135)85(142)111-59(29-33-78(132)133)86(143)116-64(43-55-24-26-56(123)27-25-55)89(146)118-67(97(154)155)40-51(2)3)119-87(144)61(31-35-80(136)137)112-84(141)58(28-32-77(130)131)113-88(145)63(42-54-18-10-7-11-19-54)117-90(147)66(45-81(138)139)110-76(129)50-107-83(140)65(44-71(100)124)109-75(128)49-106-73(126)47-104-72(125)46-105-74(127)48-108-91(148)68-21-13-38-121(68)95(152)62(20-12-36-103-98(101)102)115-93(150)69-22-14-37-120(69)94(151)57(99)41-53-16-8-6-9-17-53/h6-11,16-19,24-27,51-52,57-70,82,123H,5,12-15,20-23,28-50,99H2,1-4H3,(H2,100,124)(H,104,125)(H,105,127)(H,106,126)(H,107,140)(H,108,148)(H,109,128)(H,110,129)(H,111,142)(H,112,141)(H,113,145)(H,114,149)(H,115,150)(H,116,143)(H,117,147)(H,118,146)(H,119,144)(H,130,131)(H,132,133)(H,134,135)(H,136,137)(H,138,139)(H,154,155)(H4,101,102,103)/t52-,57+,58-,59-,60-,61-,62-,63-,64-,65-,66-,67-,68-,69-,70-,82-/m0/s1
Synonyms:- L-leucine, D-phenylalanyl-L-prolyl-L-arginyl-L-prolylglycylglycylglycylglycyl-L-asparaginylglycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-
- D-phenylalanyl-L-prolyl-L-arginyl-L-prolylglycylglycylglycylglycyl-L-asparaginylglycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucine
- Bivalirudin,TFA
- Bivalirudin Trifluoroacetate
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Found 11 products.
Bivalirudin
CAS:Bivalirudin is a highly specific and reversible direct thrombin inhibitor.Formula:C98H138N24O33Purity:98.9%Color and Shape:WhiteMolecular weight:2180.32Bivalirudin
CAS:<p>Cardiovascular drugs, not elsewhere specified or included</p>Formula:C98H138N24O33Color and Shape:White Off-White PowderMolecular weight:2178.98581L-Leucine, D-phenylalanyl-L-prolyl-L-arginyl-L-prolylglycylglycylglycylglycyl-L-asparaginylglycyl-L-α-aspartyl-L-phenylalanyl-L-α-glutamyl-L-α-glutamyl-L-isoleucyl-L-prolyl-L-α-glutamyl-L-α-glutamyl-L-tyrosyl-
CAS:Formula:C98H138N24O33Purity:98%Color and Shape:SolidMolecular weight:2180.2853Bivalirudin
CAS:Formula:C98H138N24O33Color and Shape:White To Off-White SolidMolecular weight:2180.32Bivalirudin Trifluoroacetate
CAS:Formula:C98H138N24O33Purity:95%~99%Color and Shape:White to Off-white PowderMolecular weight:2180.29Bivalirudin
CAS:<p>Bivalirudin (BG-8967) is a reversible inhibitor of α- and ζ-thrombin (Kis = 2.56 and 1.84 nM, respectively), enzymes that exhibit high fibrinogen-clotting</p>Formula:C98H138N24O33Purity:98.8% - >99.99%Color and Shape:White To Off-White PowderMolecular weight:2180.29Bivalirudin
CAS:<p>Bivalirudin is a synthetic cyclic peptide that binds to the ATP-binding cassette transporter and inhibits the activity of the proteolytic enzyme, angiotensin-converting enzyme (ACE). ACE inhibition prevents the conversion of angiotensin I to angiotensin II. Bivalirudin has been shown to be effective in reducing mortality in patients with acute coronary syndrome or undergoing percutaneous coronary intervention. It has also been shown to have pharmacokinetic properties that are similar to those of heparin. The drug has a low dose and is not associated with an increased risk of bleeding. Bivalirudin is an inhibitor and can cause drug interactions when combined with other drugs that are inhibitors or substrates for this type of transporter.</p>Formula:C98H138N24O33Purity:Min. 95%Molecular weight:2,180.33 g/molBivalirudin
CAS:<p>Selectively inhibits α- and ζ-thrombins and elicits procoagulant effects. Reduces platelet deposition in a rat carotid endarterectomy model. Has therapeutic potential as an anti-thrombotic agent in patients with heparin-associated thrombosis.</p>Formula:C98H138N24O33Purity:Min. 95%Color and Shape:White SolidMolecular weight:2178.98581Bivalirudin 1-11 Fragment Trifluoroacetic Acid Salt
CAS:Controlled Product<p>Applications Bivalirudin 1-11 Fragment is an impurity of Bivalirudin, a direct thrombin inhibitor acting as an anticoagulant through inhibition of the enzyme thrombin.<br>References Bertrand, O. et al.: Am. J. Cardio., 110, 599 (2012); Patti, G. et al.: Am. J. Cardio., 110, 478 (2012)<br></p>Formula:C43H63N15O15·(C2HF3O2)xColor and Shape:NeatMolecular weight:1030.0511402










