Ticagrelor: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
Line 4: Line 4:
| verifiedrevid = 443228756
| verifiedrevid = 443228756
| IUPAC_name = (1''S'',2''S'',3''R'',5''S'')-3-[7-[(1''R'',2''S'')-2-(3,4-Difluorophenyl)cyclopropylamino]-5-(propylthio)- 3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl]-5-(2-hydroxyethoxy)cyclopentane-1,2-diol
| IUPAC_name = (1''S'',2''S'',3''R'',5''S'')-3-[7-[(1''R'',2''S'')-2-(3,4-Difluorophenyl)cyclopropylamino]-5-(propylthio)- 3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl]-5-(2-hydroxyethoxy)cyclopentane-1,2-diol
|
| image = Ticagrelor 01.png
 
{|
| [[File:Ticagrelor_01.png|thumb|600px]]
|}image = Ticagrelor3.png
| width = 300
| width = 300
| image2 = Ticagrelor ball-and-stick animation.gif


<!--Clinical data-->
<!--Clinical data-->

Revision as of 19:20, 19 March 2014

Ticagrelor
Clinical data
Trade namesBrilinta, Brilique, Possia
SynonymsAZD-6140
MedlinePlusa611050
[[Regulation of therapeutic goods |Template:Engvar data]]
Pregnancy
category
  • US: C (Risk not ruled out)
Routes of
administration
Oral
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability36%
Protein binding>99.7%
MetabolismHepatic (CYP3A4)
Elimination half-life7 hrs (ticagrelor), 8.5 hrs (active metabolite AR-C124910XX)
ExcretionBiliary
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
E number{{#property:P628}}
ECHA InfoCard{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
FormulaC23H28F2N6O4S
Molar mass522.567 g/mol
3D model (JSmol)
 ☒N☑Y (what is this?)  (verify)


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Jesus Rosario Hernandez, M.D. [2]

Synonyms / Brand Names: Brilinta

Overview

Ticagrelor (trade name Brilinta in the US, Brilique and Possia in the EU) is a platelet aggregation inhibitor produced by AstraZeneca. The drug was approved for use in the European Union by the European Commission on December 3, 2010.[1][2] The drug was approved by the US Food and Drug Administration on July 20, 2011.[3]

Category

P2Y12 platelet inhibitor, platelet aggregation inhibitor

Prescribing Information

Brilinta (ticagrelor) tablet

References

  1. "Assessment Report for Brilique" (PDF). European Medicines Agency. January 2011.
  2. European Public Assessment Report Possia
  3. "FDA approves blood-thinning drug Brilinta to treat acute coronary syndromes". FDA. 20 July 2011.