Synthesis and Molecular Modelling Studies of New 1,3-Diaryl-5-Oxo-Proline Derivatives as Endothelin Receptor Ligands

Autor: Luisa Materia, Giuseppe Romeo, Alfredo Cagnotto, Loredana Salerno, Maria N. Modica, Valeria Pittalà, Mario Salmona, Sebastiano Intagliata, Agostino Marrazzo, Mohamed A. Helal
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Models
Molecular

Stereochemistry
homology modeling
Molecular Conformation
Pharmaceutical Science
Chemistry Techniques
Synthetic

Ligands
Article
Analytical Chemistry
ETA ligands
lcsh:QD241-441
03 medical and health sciences
0302 clinical medicine
lcsh:Organic chemistry
Drug Discovery
medicine
Molecule
Homology modeling
Physical and Theoretical Chemistry
030304 developmental biology
1
3-diaryl-5-oxo-proline derivatives

endothelin receptors
molecular docking
0303 health sciences
Binding Sites
Molecular Structure
Chemistry
Ligand
Spectrum Analysis
Organic Chemistry
Atrasentan
Antagonist
Dipeptides
Receptor
Endothelin A

Chemistry (miscellaneous)
3-diaryl-5-oxo-proline derivatives
030220 oncology & carcinogenesis
Proton NMR
cardiovascular system
Molecular Medicine
Selectivity
Endothelin receptor
medicine.drug
Protein Binding
Zdroj: Molecules
Molecules, Vol 25, Iss 1851, p 1851 (2020)
Volume 25
Issue 8
Popis: The synthesis of seventeen new 1,3-diaryl-5-oxo-proline derivatives as endothelin receptor (ETR) ligands is described. The structural configuration of the new molecules was determined by analyzing selected signals in proton NMR spectra. In vitro binding assays of the human ETA and ETB receptors allowed us to identify compound 31h as a selective ETAR ligand. The molecular docking of the selected compounds and the ETA antagonist atrasentan in the ETAR homology model provided insight into the structural elements required for the affinity and the selectivity of the ETAR subtype.
Databáze: OpenAIRE