Panzeri, Silvia and Arosio, Daniela and Gazzola, Silvia and Belvisi, Laura and Civera, Monica and Potenza, Donatella and Vasile, Francesca and Kemker, Isabell and Ertl, Thomas and Sewald, Norbert and Reiser, Oliver and Piarulli, Umberto (2020) Cyclic RGD and isoDGR Integrin Ligands Containing cis-2-amino-1-cyclopentanecarboxylic (cis-beta-ACPC) Scaffolds. MOLECULES, 25 (24): 5966. ISSN , 1420-3049
Full text not available from this repository. (Request a copy)Abstract
Integrin ligands containing the tripeptide sequences Arg-Gly-Asp (RGD) and iso-Asp-Gly- Arg (isoDGR) were actively investigated as inhibitors of tumor angiogenesis and directing unit in tumor-targeting drug conjugates. Reported herein is the synthesis, of two RGD and one isoDGR cyclic peptidomimetics containing (1S,2R) and (1R,2S) cis-2-amino-1-cyclopentanecarboxylic acid (cis-beta-ACPC), using a mixed solid phase/solution phase synthetic protocol. The three ligands were examined in vitro in competitive binding assays to the purified alpha(v)beta(3) and alpha(5)beta(1) receptors using biotinylated vitronectin (alpha(v)beta(3)) and fibronectin (alpha(5)beta(1)) as natural displaced ligands. The IC50 values of the ligands ranged from nanomolar (the two RGD ligands) to micromolar (the isoDGR ligand) with a pronounced selectivity for alpha(v)beta(3) over alpha(5)beta(1). In vitro cell adhesion assays were also performed using the human skin melanoma cell line WM115 (rich in integrin alpha(v)beta(3)). The two RGD ligands showed IC50 values in the same micromolar range as the reference compound (cyclo[RGDfV]), while for the isoDGR derivative an IC50 value could not be measured for the cell adhesion assay. A conformational analysis of the free RGD and isoDGR ligands by NMR (VT-NMR and NOESY experiments) and computational studies (MC/EM and MD), followed by docking simulations performed in the alpha(V)beta(3) integrin active site, provided a rationale for the behavior of these ligands toward the receptor.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | BIFUNCTIONAL DIKETOPIPERAZINE SCAFFOLDS; BIOLOGICAL EVALUATION; ASYMMETRIC-SYNTHESIS; MOLECULAR-MECHANICS; PEPTIDOMIMETICS; PEPTIDES; ACID; ALPHA-V-BETA-3; SELECTIVITY; ANTAGONISTS; peptidomimetics; integrin ligands; beta-amino acids; NMR conformational analysis |
| Subjects: | 500 Science > 540 Chemistry & allied sciences |
| Divisions: | Chemistry and Pharmacy > Institut für Organische Chemie Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 05 Mar 2021 09:54 |
| Last Modified: | 05 Mar 2021 09:54 |
| URI: | https://pred.uni-regensburg.de/id/eprint/43229 |
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