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vorapaxar
Known as:
[(1R,3aR,4aR,6R,8aR,9S,9aS)-9-{(E)-2-[5-(3-Fluorophényl)-2-pyridinyl]vinyl}-1-méthyl-3-oxododécahydronaphto[2,3-c]furan-6-yl]carbamate d'éthyle
, Carbamic acid, N-[(1R,3aR,4aR,6R,8aR,9S,9aS)-9-[(E)-2-[5-(3-fluorophenyl)-2-pyridinyl]ethenyl]dodecahydro-1-methyl-3-oxonaphtho[2,3-c]furan-6-yl]-, ethyl ester
, Ethyl N-[(3R,3aS,4S,4aR,7R,8aR,9aR)-4-[(E)-2-[5-(3-fluorophenyl)-2-pyridyl]vinyl]-3-methyl-1-oxo-3a,4,4a,5,6,7,8,8a,9,9a-decahydro-3H-benzo[f]isobenzofuran-7-yl]carbamate
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National Institutes of Health
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Related topics
Related topics
6 relations
Broader (3)
Lactones
Platelet Aggregation Inhibitors
Pyridines
Narrower (2)
SCH-530348
vorapaxar sulfate
vorapaxar 2.08 MG Oral Tablet [Zontivity]
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Efficacy and safety of more potent antiplatelet therapy with vorapaxar in patients with impaired renal function
Simon Correa
,
M. Bonaca
,
+4 authors
M. O’Donoghue
Journal of Thrombosis and Thrombolysis
2018
Corpus ID: 54435380
Patients with renal disease are often undertreated with antiplatelet therapy due to concerns about bleeding. Vorapaxar blocks…
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Review
2018
Review
2018
The PAR 1 antagonist , SCH 79797 , alters platelet morphology and function indepen-dently of PARs
Hannah Lee
,
R. Hamilton
2018
Corpus ID: 4137502
doi:10.1160/TH12-06-0389 Thromb Haemost 2013; 109: 164–167 Dear Sirs, Protease-activated receptors (PARs) are a family of four G…
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2017
2017
Abstract 15480: The Efficacy and Safety of More Potent Antiplatelet Therapy With Vorapaxar in Patients With Impaired Renal Function: Insights From the TRA 2P-TIMI 50 Trial
S. Gaviria
,
E. Braunwald
,
+4 authors
M. O’Donoghue
2017
Corpus ID: 81352201
Introduction: Patients with renal disease are often undertreated with antiplatelet therapy due to concerns about bleeding…
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2017
2017
Ischaemic disorders: Safe path to thrombosis prevention
Sarah Crunkhorn
Nature reviews. Drug discovery
2017
Corpus ID: 7390119
effectively reduce atherothrombotic events in patients at high risk, but the use of such agents has been associated with a risk…
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Review
2015
Review
2015
PAR 1 Receptor / Protein Interactions 1 From Multiple PAR 1 Receptor / Protein Interactions to their Multiple Therapeutic Implications
M. Gutiérrez-Rodríguez
,
R. Herranz
2015
Corpus ID: 160018597
PAR1, member of the family of protease-activated receptors, is a GPCR whose activation requires a proteolytic cleavage at its…
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2015
2015
Vorapaxar, a novel oral antiplatelet drug
Kranti Tekulapally
2015
Corpus ID: 71555739
Vorapaxor is first in the class of protease activated receptor 1 (PAR 1) antagonists. It acts by inhibiting the binding of…
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2015
2015
Vorapaxar Has Greater Net Benefit in Patients with Diabetes
H. Herrmann
2015
Corpus ID: 74617071
Vorapaxar is a new type of antiplatelet agent that blocks thrombin-induced activation at the protease activated receptor 1. In…
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Review
2013
Review
2013
High on-treatment platelet reactivity - why should we be concerned?
K. Huber
,
K. Schrör
Thrombosis and Haemostasis
2013
Corpus ID: 1452868
Antiplatelet drugs are the cornerstone in prevention and treatment of atherothrombotic vessel occlusions, i.e. myocardial…
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2012
2012
Vorapaxar expands antiplatelet options.
D. Duerschmied
,
C. Bode
Hämostaseologie
2012
Corpus ID: 47249516
Vorapaxar is the first substance of a new class of antiplatelet drugs that has been tested in large clinical trials. The protease…
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2010
2010
Identification of Human Liver Cytochrome P450 Enzymes Involved in the Metabolism of SCH 530348 (Vorapaxar), a Potent Oral Thrombin (PAR1) Receptor Antagonist
A. Ghosal
,
Xiaowen Lu
,
+5 authors
K. Alton
2010
Corpus ID: 35662820
Vorapaxar (SCH 530348), a potent oral thrombin receptor (PAR-1) antagonist, is being developed as an antiplatelet agent for…
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