Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8294890 | Biochemical and Biophysical Research Communications | 2018 | 25 Pages |
Abstract
The kinase MEKK2 (MAP3K2) activates the MEK5/ERK5 cell signaling pathway and may play an important role in tumor growth and metastasis. Thus, MEKK2 may represent a novel kinase target for cancer. In order to identify inhibitors of MEKK2, we screened a library of compounds using a high throughput MEKK2 intrinsic ATPase enzyme assay. We identified two hits with validated structures and confirmed activity in the primary assay (IC50 valuesâ¯=â¯322â¯nM and 7.7â¯Î¼M) and two orthogonal MEKK2 biochemical assays. Compound 1, the more potent hit, was the subject of further investigation. Limited structure-activity relationship (SAR) studies were performed on this iminocoumarin hit which resulted in â¥20-fold more potent analogs (e.g. 8 and 16â¯nM IC50). Two analogs had improved selectivity in a 50-member kinase profiling panel compared to the hit. These studies suggested that substitutions around the phenoxy ring of this scaffold can impart improved potency and selectivity for MEKK2. Analog Compound 1s (16â¯nM IC50) was further verified by external testing to inhibit MEKK2 and MEKK3 with similar potencies. Compound 1s displayed activity in cell-based assays in which it inhibited ERK5 pathway activation in cells and inhibited cell migration in a scratch assay. Thus, we have identified a scaffold that has promising potential to be developed into a highly selective and potent inhibitor of MEKK2. Information from these SAR studies provides specific guidance for the future design of MEKK2 inhibitor probes.
Keywords
MEKK2TR-FRETSARHTSADPDMSOMAPKAdenosine TriphosphateATPadenosine diphosphateTime-resolved fluorescence resonance energy transferstandard deviationInhibitorEnzyme-linked immunosorbent assayELISADimethyl sulfoxideStructure-activity relationshipMass spectrometryhigh throughput screeningmitogen-activated protein kinaseKinase
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Authors
Syed Ahmad, Valentine R. St. Hilaire, Srinivasa R. Dandepally, Gary L. Johnson, Alfred L. Williams, John E. Scott,