About: Ticagrelor

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An Entity of Type : http://linked.opendata.cz/ontology/drugbank/Drug, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	http://linked.opendata.cz/ontology/drugbank/Drug
http://linked.open...gbank/description	Ticagrelor (trade name Brilinta in the US, Brilique and Possia in the EU) is a platelet aggregation inhibitor produced by AstraZeneca. Unlike clopidogrel, ticagrelor is not a prodrug and does not require metabolic activation. The drug was approved for use in the European Union by the European Commission on December 3, 2010. The drug was approved by the US Food and Drug Administration on July 20, 2011. (en)
http://linked.open...y/drugbank/dosage	http://linked.opendata.cz/resource/drugbank/dosage/271B569B-363D-11E5-9242-09173F13E4C5
http://linked.open...generalReferences	# FDA label (en)
http://linked.open...gy/drugbank/group	approved (en)
http://linked.open...drugbank/halfLife	Ticagrelor has a half life of 7 hours, while its active metabolite has a half life of 9 hours. (en)
http://linked.open...ugbank/indication	For the prevention of thrombotic events (for example stroke or heart attack) in patients with acute coronary syndrome or myocardial infarction with ST elevation. (en)
sameAs	Ticagrelor Ticagrelor
Title	Ticagrelor (en)
adms:identifier	http://linked.opendata.cz/resource/drugbank/drug/DB08816/identifier/drugbank/DB08816 http://linked.opendata.cz/resource/drugbank/drug/DB08816/identifier/kegg-drug/D09017 http://linked.opendata.cz/resource/drugbank/drug/DB08816/identifier/national-drug-code-directory/0186-0777-08 http://linked.opendata.cz/resource/drugbank/drug/DB08816/identifier/wikipedia/Ticagrelor
http://linked.open...mechanismOfAction	Like the thienopyridines prasugrel, clopidogrel and ticlopidine, ticagrelor blocks adenosine diphosphate (ADP) receptors of subtype P2Y12. In contrast to the other antiplatelet drugs, ticagrelor has a binding site different from ADP, making it an allosteric antagonist, and the blockage is reversible. Moreover, the drug does not need hepatic activation, which might work better for patients with genetic variants regarding the enzyme CYP2C19 (although it is not certain whether clopidogrel is significantly influenced by such variants). (en)
http://linked.open...y/drugbank/patent	http://linked.opendata.cz/resource/drugbank/patent/2296665 http://linked.opendata.cz/resource/drugbank/patent/2351709%20 http://linked.opendata.cz/resource/drugbank/patent/2408596
http://linked.open...outeOfElimination	The primary route of ticagrelor elimination is hepatic metabolism. When radiolabeled ticagrelor is administered, the mean recovery of radioactivity is approximately 84% (58% in feces, 26% in urine). (en)
http://linked.open.../drugbank/synonym	AZD6140 (en) AZD 6140 (en) AZD-6140 (en) Brilinta (en) (1S,2S,3R,5S)-3-(7-((1R,2S)-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 (en)
http://linked.open...drugbank/toxicity	Bleeding is the expected pharmacologic effect of overdosing. If bleeding occurs, appropriate supportive measures should be taken. Other effects of overdose may include gastrointestinal effects (nausea, vomiting, diarrhea) or ventricular pauses. (en)
http://linked.open...umeOfDistribution	The steady state volume of distribution of ticagrelor is 88 L. (en)
http://linked.open.../drug/hasAHFSCode	http://linked.opendata.cz/resource/AHFS/20-12-18%20
http://linked.open...nk/proteinBinding	Both ticagrelor and AR-C124910XX are bound to plasma proteins (>99.7%), and both are pharmacologically active. (en)
http://linked.open...ynthesisReference	Anil Shahaji Khile, "NOVEL PROCESSES FOR THE PREPARATION OF PHENYLCYCLOPROPYLAMINE DERIVATIVES AND USE THEREOF FOR PREPARING TICAGRELOR." U.S. Patent US20130165696, issued June 27, 2013. (en)
foaf:page	http://www.drugs.com/cdi/ticagrelor.html http://www.rxlist.com/brilinta-drug.htm
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http://linked.open...l/drug/hasATCCode	Ticagrelor
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http://linked.open...ugbank/absorption	Absorbed quickly from the gut, the bioavailability being 36%. (en)
http://linked.open.../affectedOrganism	Humans and other mammals (en)
http://linked.open...casRegistryNumber	274693-27-5 (en)
http://linked.open...drugbank/category	(en)
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