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Tranexamic Acid

Catalog No. DB00302 Name DrugBank
CAS Number 1197-18-8 Website http://www.ualberta.ca/
M. F. C8H15NO2 Telephone (780) 492-3111
M. W. 157.2102 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 187

SYNONYMS

IUPAC name
4-(aminomethyl)cyclohexane-1-carboxylic acid
IUPAC Traditional name
tranexamic acid
Brand Name
Amstat
Mastop
Amikapron
Cyklokapron
Emorhalt
Frenolyse
Rikavarin
Rikavarin-S
Tamcha
Ugurol
Amcha
Anvitoff
Carxamin
Cyclocapron
Tranexan
Transamin
Trasamlon
Synonyms
tranexmic acid
Trans AMCHA
trans-4-aminomethylcyclohexane-1-carboxylic acid
Tranexamsaeure
Tranhexamic acid
trans-Tranexamic acid
trans-Amcha

DATABASE IDS

CAS Number 1197-18-8

PROPERTIES

Hydrophobicity(logP) 0.3
Solubility 1.67E+005 mg/L

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Antifibrinolytic hemostatic used in severe hemorrhage. [PubChem]
Indication For use in patients with hemophilia for short term use (two to eight days) to reduce or prevent hemorrhage and reduce the need for replacement therapy during and following tooth extraction. It can also be used for excessive bleeding in menstruation, surgery, or trauma cases.
Pharmacology Tranexamic acid is an antifibrinolytic that competitively inhibits the activation of plasminogen to plasmin. Tranexamic acid is a competitive inhibitor of plasminogen activation, and at much higher concentrations, a noncompetitive inhibitor of plasmin, i.e., actions similar to aminocaproic acid. Tranexamic acid is about 10 times more potent in vitro than aminocaproic acid. Tranexamic acid binds more strongly than aminocaproic acid to both the strong and weak receptor sites of the plasminogen molecule in a ratio corresponding to the difference in potency between the compounds. Tranexamic acid in a concentration of 1 mg per mL does not aggregate platelets in vitro. In patients with hereditary angioedema, inhibition of the formation and activity of plasmin by tranexamic acid may prevent attacks of angioedema by decreasing plasmin-induced activation of the first complement protein (C1).
Toxicity Oral LD50 in mice is >10 gm/kg. Symptoms of overdosage may be nausea, vomiting, orthostatic symptoms and/or hypotension.
Affected Organisms
Humans and other mammals
Biotransformation Only a small fraction of the drug is metabolized (less than 5%).
Absorption Absorption of tranexamic acid after oral administration in humans represents approximately 30 to 50% of the ingested dose and bioavailability is not affected by food intake.
Half Life Biological half-life in the joint fluid is about 3 hours.
Protein Binding The plasma protein binding of tranexamic acid is about 3% at therapeutic plasma levels and seems to be fully accounted for by its binding to plasminogen (does not bind serum albumin).
Elimination Urinary excretion is the main route of elimination via glomerular filtration.
Distribution * 9 to 12 L
Clearance * 110 - 116 mL/min
External Links
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REFERENCES