All Stories

  1. Angiotensin II cyclic analogs as tools to investigate AT 1 R biased signaling mechanisms
  2. Structural Optimization and Characterization of Potent Analgesic Macrocyclic Analogues of Neurotensin (8–13)
  3. Label-free cell signaling pathway deconvolution of Angiotensin type 1 receptor reveals time-resolved G-protein activity and distinct AngII and AngIII\IV responses
  4. The hypotensive effect of activated apelin receptor is correlated with β-arrestin recruitment
  5. In Search of the Optimal Macrocyclization Site for Neurotensin
  6. Agonist-Antagonist Transition in CXCR4 Ligands
  7. Use of Molecular Modeling to Design Selective NTS2 Neurotensin Analogues
  8. The signaling signature of the neurotensin type 1 receptor with endogenous ligands
  9. Structure–activity relationship of novel macrocyclic biased apelin receptor agonists
  10. Identification of 2-({[1-(4-Fluorophenyl)-5-(2-methoxyphenyl)-1H-pyrazol-3-yl]carbonyl}amino)tricyclo[3.3.1.13,7]decane-2-carboxylic Acid (NTRC-844) as a Selective Antagonist for the Rat Neurotensin Receptor Type 2
  11. Structure–Activity Relationship and Signaling of New Chimeric CXCR4 Agonists
  12. Discovery and Structure–Activity Relationship of a Bioactive Fragment of ELABELA that Modulates Vascular and Cardiac Functions
  13. Stereoselective Synthesis of β-(5-Arylthiazolyl) α-Amino Acids and Use in Neurotensin Analogues
  14. Design, synthesis, and biological evaluation of CXCR4 ligands
  15. Synthesis and Characterization in Vitro and in Vivo of (l)-(Trimethylsilyl)alanine Containing Neurotensin Analogues
  16. C-Terminal Modifications of Apelin-13 Significantly Change Ligand Binding, Receptor Signaling, and Hypotensive Action
  17. Conjugation of a brain-penetrant peptide with neurotensin provides antinociceptive properties
  18. Synthetic Agonists for the CXCR4 Receptor: SAR, Signaling Pathways and Peptidomimetic Transition
  19. Elucidation of the Structure-Activity Relationships of Apelin: Influence of Unnatural Amino Acids on Binding, Signaling, and Plasma Stability