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Development of new Malt1 inhibitors and probes

Authors :
Christoph Driessen
Herman S. Overkleeft
Bo-Tao Xin
Daniel Krappmann
Bogdan I. Florea
Yimeng Du
Gijsbert A. van der Marel
Gisela Schimmack
Source :
Bioorganic & Medicinal Chemistry. 24:3312-3329
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

Mucosa-associated lymphoid tissue lymphoma translocation protein 1 (Malt1) is a promising therapeutic target for the treatment of activated B cell-like diffuse large B cell lymphoma (ABC-DLBCL). Several research groups have reported on the development of Malt1 inhibitors and activity-based probes for in vitro and in situ monitoring and modulating Malt1 activity. In this paper, we report on two activity-based Malt1 probes (6 and 7) and a focused library of 19 new Malt1 inhibitors. Our peptide-based probe 6 labels Malt1 in an activity-based manner. In contrast, probe 7, derived from the known covalent inhibitor MI-2, labels both wild type and catalytically inactive Cys to Ala mutant Malt1, suggesting that MI-2 inhibits Malt1 by reacting with a nucleophilic residue other than the active site cysteine. Furthermore, two of our inhibitors (9, apparent IC50 3.0μM, and 13, apparent IC50 2.1μM) show good inhibitory activity against Malt1 and outperform MI-2 (apparent IC50 7.8μM) in our competitive activity-based protein profiling assay.

Details

ISSN :
09680896
Volume :
24
Database :
OpenAIRE
Journal :
Bioorganic & Medicinal Chemistry
Accession number :
edsair.doi.dedup.....6e755930a9b42a969ffe1e4cef40fabc