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191588-94-0

191588-94-0 Structure

191588-94-0 Structure
IdentificationBack Directory
[Name]

tenecteplase
[CAS]

191588-94-0
[Synonyms]

Tnkase
Tnk-tpa
tenecteplase
Unii-wgd229o42w
Research Grade Tenecteplase (DHB88401)
Plasminogen activator(human tissue-type),103-L-asparagine-117-L-glutamine-296-L-alanine-297-L-alanine-298-L-alanine-299-L-alanine-
Plasminogen activator (human tissue-type), 103-L-asparagine-117-L-glutamine-296-L-alanine-297-L-alanine-298-L-alanine-299-alanine-
Chemical PropertiesBack Directory
[form ]

Liquid
[color ]

Colorless to light yellow
Hazard InformationBack Directory
[Uses]

Treatment of acute thrombotic disorders.
[General Description]

Tenecteplase is a tPA produced by recombinant CHO cells.The molecule is a 527-amino acid glycoprotein developed byintroducing the following modifications to the cDNA construct:Thr103 to Asp, Asp117 to Gln, both within the kringle-1domain, and a tetra-alanine substitution at amino acids 296 to299 in the protease domain. The drug is a sterile, lyophilizedpowder recommended for single IV bolus administration afterreconstitution with sterile water. Tenecteplase should be administeredimmediately after reconstitution.
[Mechanism of action]

Tenecteplase is composed of 527 amino acids with 17 disulfide bridges. It differs structurally from anteplase by three point mutations. The mutations were bioengineered to occur at amino acid 103, where threonine (T) is replaced by asparagine; at amino acid 117, where asparagine (N) is replaced by glutamine; and at amino acids 296 to 299, where lysine (K)-histidinearginine-arginine are replaced with four alanines. Thus, the name TNK is derived from the mutations. The replacement of these amino acids along with their attached carbohydrate side chains results in a prolonged half-life (~17 minutes) and allows a single bolus application. These point-mutation changes also change the binding of tenecteplase to plasminogen activator inhibitor-1 (PAI-1) by 80-fold, thus improving activity. A physiological enzyme, PAI-1 inhibits fibrinolysis. Finally, tenecteplase shows a 15-fold higher fibrin specificity. The drug is still eliminated via hepatic mechanisms.
[Clinical Use]

Thrombolytic:
Acute myocardial infarction
[Drug interactions]

Potentially hazardous interactions with other drugs
Drugs that affect coagulation or platelet function: increased risk of bleeding.
[Metabolism]

Tenecteplase is cleared from circulation by binding to specific receptors in the liver followed by catabolism to small peptides.
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