Xavier Sainsily
Sherbrooke, QC, Canada
Last Updated: 09/26/2026
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Found 13 publications
Size-Reduced Macrocyclic Analogues of [Pyr1]-apelin-13 Showing Negative Gα12 Bias Still Produce Prolonged Cardiac Effects.
Journal: Journal of medicinal chemistry
Published: January 04, 2022
Elabela Protects Spontaneously Hypertensive Rats From Hypertension and Cardiorenal Dysfunctions Exacerbated by Dietary High-Salt Intake.
Journal: Frontiers in pharmacology
Published: May 14, 2021
Apelin-13 in septic shock: effective in supporting hemodynamics in sheep but compromised by enzymatic breakdown in patients.
Journal: Scientific reports
Published: March 30, 2021
Gαi-biased apelin analog protects against isoproterenol-induced myocardial dysfunction in rats.
Journal: American journal of physiology. Heart and circulatory physiology
Published: February 26, 2021
Constraining the Side Chain of C-Terminal Amino Acids in Apelin-13 Greatly Increases Affinity, Modulates Signaling, and Improves the Pharmacokinetic Profile.
Journal: Journal of medicinal chemistry
Published: February 01, 2021
Structure-Activity Relationship and Bioactivity of Short Analogues of ELABELA as Agonists of the Apelin Receptor.
Journal: Journal of medicinal chemistry
Published: December 22, 2020
A Systematic Exploration of Macrocyclization in Apelin-13: Impact on Binding, Signaling, Stability, and Cardiovascular Effects.
Journal: Journal of medicinal chemistry
Published: February 21, 2018
The apelinergic system as an alternative to catecholamines in low-output septic shock.
Journal: Critical care (London, England)
Published: November 07, 2017
ELABELA Improves Cardio-Renal Outcome in Fatal Experimental Septic Shock.
Journal: Critical care medicine
Published: August 05, 2017
Structure-activity relationship of novel macrocyclic biased apelin receptor agonists.
Journal: Organic & biomolecular chemistry
Published: December 08, 2016
Discovery and Structure-Activity Relationship of a Bioactive Fragment of ELABELA that Modulates Vascular and Cardiac Functions.
Journal: Journal of medicinal chemistry
Published: March 18, 2016
Identification of transmembrane domain 1 & 2 residues that contribute to the formation of the ligand-binding pocket of the urotensin-II receptor.
Journal: Biochemical pharmacology
Published: June 19, 2014
Last Updated: 09/26/2026