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- 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