PT  - JOURNAL ARTICLE
AU  - Tyler S. Beyett
AU  - Xinmin Gan
AU  - Shannon M. Reilly
AU  - Louise Chang
AU  - Andrew V. Gomez
AU  - Alan R. Saltiel
AU  - Hollis D. Showalter
AU  - John J. G. Tesmer
TI  - Carboxylic Acid Derivatives of Amlexanox Display Enhanced Potency toward TBK1 and IKK<em>ε</em> and Reveal Mechanisms for Selective Inhibition
AID  - 10.1124/mol.118.112185
DP  - 2018 Oct 01
TA  - Molecular Pharmacology
PG  - 1210--1219
VI  - 94
IP  - 4
4099  - http://molpharm.aspetjournals.org/content/94/4/1210.short
4100  - http://molpharm.aspetjournals.org/content/94/4/1210.full
SO  - Mol Pharmacol2018 Oct 01; 94
AB  - Chronic low-grade inflammation is a hallmark of obesity, which is a risk factor for the development of type 2 diabetes. The drug amlexanox inhibits IκB kinase ε (IKKε) and TANK binding kinase 1 (TBK1) to promote energy expenditure and improve insulin sensitivity. Clinical studies have demonstrated efficacy in a subset of diabetic patients with underlying adipose tissue inflammation, albeit with moderate potency, necessitating the need for improved analogs. Herein we report crystal structures of TBK1 in complex with amlexanox and a series of analogs that modify its carboxylic acid moiety. Removal of the carboxylic acid or mutation of the adjacent Thr156 residue significantly reduces potency toward TBK1, whereas conversion to a short amide or ester nearly abolishes the inhibitory effects. IKKε is less affected by these modifications, possibly due to variation in its hinge that allows for increased conformational plasticity. Installation of a tetrazole carboxylic acid bioisostere improved potency to 200 and 400 nM toward IKKε and TBK1, respectively. Despite improvements in the in vitro potency, no analog produced a greater response in adipocytes than amlexanox, perhaps because of altered absorption and distribution. The structure-activity relationships and cocrystal structures described herein will aid in future structure-guided inhibitor development using the amlexanox pharmacophore for the treatment of obesity and type 2 diabetes.