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Pallesen, J.S.* ; Narayanan, D.* ; Tran, K.T.* ; Solbak, S.M.* ; Marseglia, G.* ; Sørensen, L.M.E.* ; Høj, L.J.* ; Munafò, F.* ; Carmona, R.M.C.* ; Garcia, A.D.* ; Desu, H.L.* ; Brambilla, R.* ; Johansen, T.N.* ; Popowicz, G.M. ; Sattler, M. ; Gajhede, M.* ; Bach, A.*

Deconstructing noncovalent kelch-like ECH-associated protein 1 (Keap1) inhibitors into fragments to reconstruct new potent compounds.

J. Med. Chem. 64, 4623-4661 (2021)
Postprint DOI
Open Access Green
Targeting the protein-protein interaction (PPI) between nuclear factor erythroid 2-related factor 2 (Nrf2) and Kelch-like ECH-associated protein 1 (Keap1) is a potential therapeutic strategy to control diseases involving oxidative stress. Here, six classes of known small-molecule Keap1-Nrf2 PPI inhibitors were dissected into 77 fragments in a fragment-based deconstruction reconstruction (FBDR) study and tested in four orthogonal assays. This gave 17 fragment hits of which six were shown by X-ray crystallography to bind in the Keap1 Kelch binding pocket. Two hits were merged into compound 8 with a 220-380-fold stronger affinity (Ki = 16 μM) relative to the parent fragments. Systematic optimization resulted in several novel analogues with Ki values of 0.04-0.5 μM, binding modes determined by X-ray crystallography, and enhanced microsomal stability. This demonstrates how FBDR can be used to find new fragment hits, elucidate important ligand-protein interactions, and identify new potent inhibitors of the Keap1-Nrf2 PPI.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Macromolecular Crystallography Beamline; Kinetic/affinity Interaction Constants; Fluorescence Polarization; Small-molecule; Oxidative Stress; Diffusion-coefficients; Keap1-nrf2-are Pathway; Nrf2; Binding; Discovery
ISSN (print) / ISBN 0022-2623
e-ISSN 1520-4804
Quellenangaben Band: 64, Heft: 8, Seiten: 4623-4661 Artikelnummer: , Supplement: ,
Verlag American Chemical Society (ACS)
Verlagsort 1155 16th St, Nw, Washington, Dc 20036 Usa
Begutachtungsstatus Peer reviewed
Förderungen Accelerated Early staGe drug dIScovery (AEGIS)
A. P. Moller Foundation for the Advancement of Medical Science
Horslev Foundation
Augustinus Foundation
European Union's Framework Program for Research and Innovation Horizon 2020 (2014-2020) under the Marie SklodowskaCurie Grant
Helmholtz Center Munich
Danish Research Council for Independent Research\Nature and Universe
Drug Research Academy/Lundbeck Foundation
Lundbeck Foundation