Results
Title

Shifting Towards α<sub>V</sub>β<sub>6</sub> Integrin Ligands Using Novel Aminoproline‐Based Cyclic Peptidomimetics.

Authors

Bugatti, Kelly; Bruno, Agostino; Arosio, Daniela; Sartori, Andrea; Curti, Claudio; Augustijn, Lisa; Zanardi, Franca; Battistini, Lucia

Abstract

In recognition of the key role played by integrins in several life‐threatening dysfunctions, the search for novel small‐molecule probes that selectively recognize these surface receptors is still open and widely pursued. Inspired by previously established aminoproline (Amp)‐RGD based cyclopeptidomimetics with attracting αVβ3 integrin affinity and selectivity, the design and straightforward synthesis of 18 new AmpRGD chemotypes bearing additional structural variants were herein implemented, to shift toward peptide‐like αVβ6 integrin targeted binders. The ligand competence of the synthesized products toward αVβ6 was evaluated in competitive binding assays on isolated receptors, and αVβ6/αVβ3 selectivity was determined for a subgroup of compounds, resulting in the identification of four very promising candidates. SAR considerations and docking simulations allowed us to appreciate the key structural features responsible for the observed activity.

Subjects

PEPTIDOMIMETICS; BINDING site assay; INTEGRINS; LIGANDS (Chemistry); STRUCTURE-activity relationships

Publication

Chemistry - A European Journal, 2020, Vol 26, Issue 59, p13468

ISSN

0947-6539

Publication type

Academic Journal

DOI

10.1002/chem.202002554