Alteplase CAS 105857-23-6

Introduction:Basic information about Alteplase CAS 105857-23-6, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Alteplase Basic informationApplication in Ischemic Stroke

Product Name:Alteplase
Synonyms:Alteplase;Activase (tn);Alteplase (genetical recombination);Alteplase (genetical recombination) (jan);Alteplase (usp/inn);D02837;PlasMinogen activator (huMan tissue-type protein Moiety) (9CI);Alteplase USP/EP/BP
CAS:105857-23-6
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MW:0
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Mol File:Mol File

Alteplase Chemical Properties

form Solid
color White to off-white

Safety Information

Alteplase Usage And Synthesis

Application in Ischemic StrokeIn the therapy of Ischemic Stroke, Alteplase is initiated within 3 hours of symptom onset has been shown to reduce the ultimate disability due to ischemic stroke. A head CT scan must be obtained to rule out hemorrhage before beginning therapy.
It is administrated 0.9 mg/kg IV (maximum 90 mg) over 1 hour in selected patients within 3 hours of onset.
DescriptionAlteplase is a recombinant single-chain tissue plasminogen activator useful in themanagement of thrombosis in acute myocardial infarct. It reportedly causes no allergicreactions but requires intravenous infusion due to a short half-life. Alteplase is the onlyagent on the U.S. market indicated for the reduction of incidence of congestive heartfailure following a heart attack.
OriginatorGenentech (USA)
UsesTissue-type plasminogen activator; fibrinolytic.
Brand nameActivase (Genentech);Actilyse.
General DescriptionAlteplase (Activase) is a tissue plasminogenactivator (t-PA) produced by rDNA technology. It is a single-chain glycoprotein protease consisting of 527 aminoacid residues. Native t-PA is isolated from a melanoma cellline. The single-chain molecule is susceptible to enzymaticdigestion to a two-chain molecule, in which the two chainsremain linked with a disulfide bond. Both forms of the nativet-PA are equipotent in fibrinolytic (and plasminogenactivating)properties. It is an extrinsic plasminogen activatorassociated with vascular endothelial tissue, whichpreferentially activates plasminogen bound to fibrin. Thefibrinolytic action of alteplase (t-PA) is confined to thrombi,with minimal systemic activation of plasminogen. It is producedcommercially by rDNA methods by inserting the alteplasegene (acquired from human melanoma cells) intoovarian cells of the Chinese hamster, serving as host cells.The melanoma-derived alteplase is immunologically andchemically identical with the uterine form. Alteplase is indicatedfor the intravenous management of acute myocardialinfarction.
Mechanism of actionAs a main endogenic promoter of fibrinolysis, t-PA binds with fibrin and, like urokinase,breaks Arg-560–Val-561 peptide bond in the fibrin-binded plasminogen molecule, thusturning it into an active plasmin molecule that breaks apart fibrin clots. Its action is localizedin thrombotic regions, and thus the likelihood of systemic fibrinolysis originating duringits use is much lower than that which can originate while using streptokinase andurokinase.
Clinical UseAlteplase (tPA) is a serine protease with a low affinity for free plasminogen but a very high affinityfor theplasminogen bound to fibrin in a thrombus (fibrin-specific agent). Both streptokinaseand urokinase lack this specificity (i.e., are nonspecific) and act on free plasminogen, inducing ageneralized thrombolytic state. Alteplase also has a greater specificity for older clots compared withnewer clots relative to streptokinase and urokinase. Alteplase was originally isolated from culturesof human melanoma cells but is now produced commercially using recombinant DNA technology.
Side effectsAlteplase is unmodified human tPA, whereas reteplase is human tPA that has hadseveral specific amino acid sequences removed. At low doses, alteplase is quite selective fordegrading fibrin without concomitant lysis of other proteins, such as fibrinogen. At the higher dosescurrently used therapeutically, however, alteplase activates free plasminogen to some extent and,therefore, can cause hemorrhage. Many of the therapeutic indications for the other thrombolyticagents also are indications for alteplase (i.e., myocardial infarction, massive pulmonary embolism,and acute ischemic stroke).

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