E-64c-hydrazide based cathepsin C inhibitors: Optimizing the interactions with the S1'-S2' area
Tromsdorf N, Ullrich F, Rethmeier M, Sommerhoff C, Schaschke N (2023)
ChemMedChem: e202300218.
Zeitschriftenaufsatz
| E-Veröff. vor dem Druck | Englisch
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Autor*in
Tromsdorf, Nora;
Ullrich, Fabian;
Rethmeier, Markus;
Sommerhoff, Christian;
Schaschke, NorbertUniBi
Einrichtung
Abstract / Bemerkung
The zymogens of the neutrophil serine proteases elastase, proteinase 3, and cathepsin G are converted proteolytically into their pro-inflammatory active forms by the action of cathepsin C. The inhibition of this cysteine protease therefore is an interesting therapeutic approach for the treatment of inflammatory disorders with a high neutrophil burden such as COPD. Based on E-64c-hydrazide as lead structure, we have recently developed a covalently acting cathepsin C inhibitor using a n-butyl residue attached at the amine nitrogen of the hydrazide moiety to efficiently address the deep hydrophobic S2 pocket. To further optimize the affinity and selectivity profile of this inhibitor, the S1'-S2' area was now investigated by a combinatorial approach, showing that Nle-tryptamide is a ligand superior to the initially used Leu-isoamylamide. Using the neutrophil precursor line U937 as a cell culture model, this optimized inhibitor blocks the intracellular cathepsin C activity and thereby suppresses the activation of neutrophil elastase. © 2023 Wiley-VCH GmbH.
Erscheinungsjahr
2023
Zeitschriftentitel
ChemMedChem
Art.-Nr.
e202300218
Urheberrecht / Lizenzen
eISSN
1860-7187
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https://pub.uni-bielefeld.de/record/2981179
Zitieren
Tromsdorf N, Ullrich F, Rethmeier M, Sommerhoff C, Schaschke N. E-64c-hydrazide based cathepsin C inhibitors: Optimizing the interactions with the S1'-S2' area. ChemMedChem. 2023: e202300218.
Tromsdorf, N., Ullrich, F., Rethmeier, M., Sommerhoff, C., & Schaschke, N. (2023). E-64c-hydrazide based cathepsin C inhibitors: Optimizing the interactions with the S1'-S2' area. ChemMedChem, e202300218. https://doi.org/10.1002/cmdc.202300218
Tromsdorf, Nora, Ullrich, Fabian, Rethmeier, Markus, Sommerhoff, Christian, and Schaschke, Norbert. 2023. “E-64c-hydrazide based cathepsin C inhibitors: Optimizing the interactions with the S1'-S2' area”. ChemMedChem: e202300218.
Tromsdorf, N., Ullrich, F., Rethmeier, M., Sommerhoff, C., and Schaschke, N. (2023). E-64c-hydrazide based cathepsin C inhibitors: Optimizing the interactions with the S1'-S2' area. ChemMedChem:e202300218.
Tromsdorf, N., et al., 2023. E-64c-hydrazide based cathepsin C inhibitors: Optimizing the interactions with the S1'-S2' area. ChemMedChem, : e202300218.
N. Tromsdorf, et al., “E-64c-hydrazide based cathepsin C inhibitors: Optimizing the interactions with the S1'-S2' area”, ChemMedChem, 2023, : e202300218.
Tromsdorf, N., Ullrich, F., Rethmeier, M., Sommerhoff, C., Schaschke, N.: E-64c-hydrazide based cathepsin C inhibitors: Optimizing the interactions with the S1'-S2' area. ChemMedChem. : e202300218 (2023).
Tromsdorf, Nora, Ullrich, Fabian, Rethmeier, Markus, Sommerhoff, Christian, and Schaschke, Norbert. “E-64c-hydrazide based cathepsin C inhibitors: Optimizing the interactions with the S1'-S2' area”. ChemMedChem (2023): e202300218.
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