CAS 128270-60-0
:Bivalirudina
Descrição:
Bivalirudina é um peptídeo sintético que funciona como um inibidor direto da trombina, utilizado principalmente como anticoagulante em ambientes clínicos, particularmente durante intervenções coronárias percutâneas. Sua estrutura consiste em 20 aminoácidos e é derivada do peptídeo hirudina encontrado em sanguessugas. Bivalirudina exibe uma alta afinidade pela trombina, prevenindo efetivamente a conversão de fibrinogênio em fibrina, o que é crucial no processo de coagulação. A substância é administrada por injeção intravenosa e tem uma meia-vida relativamente curta, necessitando de monitoramento cuidadoso dos níveis de anticoagulação durante o tratamento. Bivalirudina é caracterizado por sua estabilidade na corrente sanguínea e sua capacidade de fornecer anticoagulação rápida com um perfil farmacocinético previsível. Muitas vezes é preferido em relação aos anticoagulantes tradicionais devido ao seu menor risco de induzir trombocitopenia e sua facilidade de uso em pacientes com função renal variável. No geral, Bivalirudina representa um avanço significativo na terapia anticoagulante, particularmente no manejo da síndrome coronária aguda.
Fórmula: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
Sinónimos:- 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
Ordenar por
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11 produtos.
Bivalirudin
CAS:Bivalirudin is a highly specific and reversible direct thrombin inhibitor.Fórmula:C98H138N24O33Pureza:98.9%Cor e Forma:WhitePeso molecular:2180.32Bivalirudin
CAS:Cardiovascular drugs, not elsewhere specified or includedFórmula:C98H138N24O33Cor e Forma:White Off-White PowderPeso molecular: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:Fórmula:C98H138N24O33Pureza:98%Cor e Forma:SolidPeso molecular:2180.2853Bivalirudin Trifluoroacetate
CAS:Fórmula:C98H138N24O33Pureza:95%~99%Cor e Forma:White to Off-white PowderPeso molecular: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>Fórmula:C98H138N24O33Pureza:98.8% - >99.99%Cor e Forma:White To Off-White PowderPeso molecular: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>Fórmula:C98H138N24O33Pureza:Min. 95%Peso molecular: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>Fórmula:C98H138N24O33Pureza:Min. 95%Cor e Forma:White SolidPeso molecular:2178.98581Bivalirudin 1-11 Fragment Trifluoroacetic Acid Salt
CAS:Produto Controlado<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>Fórmula:C43H63N15O15·(C2HF3O2)xCor e Forma:NeatPeso molecular:1030.0511402










