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selexipag
Known as:
2-(4-((5,6-diphenylpyrazin-2-yl)(isopropyl)amino)butoxy)-N-(methylsulfonyl)acetamide
National Institutes of Health
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Related topics
Related topics
6 relations
Narrower (3)
ACT 293987
NS-304
Uptravi
Broader (3)
Acetamides
Antihypertensive Agents
Pyrazines
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
Guidelines for the Treatment of Pulmonary Arterial Hypertension
Z. Vazquez
,
J. Klinger
Lung
2020
Corpus ID: 220543341
Pulmonary arterial hypertension (PAH) is a rare form of pulmonary hypertension characterized by a progressive obliterative…
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2020
2020
Risk assessment in pulmonary arterial hypertension: Insights from the GRIPHON study.
O. Sitbon
,
K. Chin
,
+12 authors
M. Hoeper
The Journal of Heart and Lung Transplantation
2020
Corpus ID: 59001697
2019
2019
Selexipag treatment for pulmonary arterial hypertension associated with congenital heart disease after defect correction: insights from the randomised controlled GRIPHON study
M. Beghetti
,
R. Channick
,
+12 authors
N. Galiè
European Journal of Heart Failure
2019
Corpus ID: 58586088
Patients with pulmonary arterial hypertension associated with congenital heart disease (CHD‐PAH) after defect correction have a…
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Review
2017
Review
2017
Selexipag for the treatment of pulmonary arterial hypertension.
Zachary R. Noel
,
K. Kido
,
Tracy E. Macaulay
American Journal of Health-System Pharmacy
2017
Corpus ID: 24347291
PURPOSE The pharmacology, pharmacokinetics, clinical efficacy, safety and tolerability, dosing and administration, and place in…
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Review
2017
Review
2017
Selexipag: A Review in Pulmonary Arterial Hypertension
S. Duggan
,
S. Keam
,
Celeste B. Burness
American Journal of Cardiovascular Drugs
2017
Corpus ID: 3595630
Selexipag (Uptravi®) is an orally active, first-in-class, selective prostacyclin IP receptor agonist. Selexipag was approved…
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Review
2015
Review
2015
The mechanistic basis of prostacyclin and its stable analogues in pulmonary arterial hypertension: Role of membrane versus nuclear receptors.
L. Clapp
,
R. Gurung
Prostaglandins & other lipid mediators
2015
Corpus ID: 9252269
Highly Cited
2015
Highly Cited
2015
Selexipag: An Oral and Selective IP Prostacyclin Receptor Agonist for the Treatment of Pulmonary Arterial Hypertension.
T. Asaki
,
Keiichi Kuwano
,
K. Morrison
,
J. Gatfield
,
T. Hamamoto
,
M. Clozel
Journal of Medicinal Chemistry
2015
Corpus ID: 8138938
Prostacyclin controls cardiovascular function via activation of the prostacyclin receptor. Decreased prostacyclin production…
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Highly Cited
2015
Highly Cited
2015
Pharmacokinetics and Tolerability of the Novel Oral Prostacyclin IP Receptor Agonist Selexipag
P. Kaufmann
,
K. Okubo
,
+4 authors
H. Mukai
American Journal of Cardiovascular Drugs
2015
Corpus ID: 14863287
PurposeTargeting the prostacyclin pathway is an effective treatment option for pulmonary arterial hypertension (PAH). Patients…
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Highly Cited
2014
Highly Cited
2014
Multiple-Dose Up-Titration Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Selexipag, an Orally Available Selective Prostacyclin Receptor Agonist, in Healthy…
S. Bruderer
,
N. Hurst
,
P. Kaufmann
,
J. Dingemanse
Pharmacology
2014
Corpus ID: 23274419
Objective: The objective of this study was to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of…
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2010
2010
JPET # 169748 2 RUNNING TITLE PAGE Running Title : Selexipag and gastric function Corresponding
K. Morrison
,
R. Ernst
,
P. Hess
,
R. Studer
,
M. Clozel
2010
Corpus ID: 2859575
word count: 250
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