Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1394939 | European Journal of Medicinal Chemistry | 2016 | 10 Pages |
•A series of C(5)-substituted analogues of FLAP inhibitor BRP-7 were synthesized.•5-Nitrile substitution resulted in the highly active derivative 11.•Docking studies and molecular dynamic simulations of 11 with FLAP were investigated.
Pharmacological intervention with 5-lipoxygenase (5-LO) pathway leading to suppression of leukotriene (LT) biosynthesis is a clinically validated strategy for treatment of respiratory and cardiovascular diseases such as asthma and atherosclerosis. Here we describe the synthesis of a series of C(5)-substituted analogues of the previously described 5-LO-activating protein (FLAP) inhibitor BRP-7 (IC50 = 0.31 μM) to explore the effects of substitution at the C(5)-benzimidazole (BI) ring as a strategy to increase the potency against FLAP-mediated 5-LO product formation. Incorporation of polar substituents on the C(5) position of the BI core, exemplified by compound 11 with a C(5)-nitrile substituent, significantly enhances the potency for suppression of 5-LO product synthesis in human neutrophils (IC50 = 0.07 μM) and monocytes (IC50 = 0.026 μM).
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