1. Synthesis and Evaluation of diaryl ether modulators of the leukotriene A 4 hydrolase aminopeptidase activity.
- Author
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Petruncio G, Lee KH, Girgis M, Shellnutt Z, Beaulac Z, Xiang J, Lee SH, Peng X, Burdick M, Noble SM, Shim YM, and Paige M
- Subjects
- Animals, Mice, Structure-Activity Relationship, Humans, Molecular Structure, Aminopeptidases metabolism, Aminopeptidases antagonists & inhibitors, Ethers pharmacology, Ethers chemistry, Ethers chemical synthesis, Dose-Response Relationship, Drug, Models, Molecular, Crystallography, X-Ray, Epoxide Hydrolases antagonists & inhibitors, Epoxide Hydrolases metabolism
- Abstract
Activation of the aminopeptidase (AP) activity of leukotriene A
4 hydrolase (LTA4 H) presents a potential therapeutic strategy for resolving chronic inflammation. Previously, ARM1 and derivatives were found to activate the AP activity using the alanine-p-nitroanilide (Ala-pNA) as a reporter group in an enzyme kinetics assay. As an extension of this previous work, novel ARM1 derivatives were synthesized using a palladium-catalyzed Ullmann coupling reaction and screened using the same assay. Analogue 5, an aminopyrazole (AMP) analogue of ARM1, was found to be a potent AP activator with an AC50 of 0.12 μM. An X-ray crystal structure of LTA4 H in complex with AMP was refined at 2.7 Å. Despite its AP activity with Ala-pNA substrate, AMP did not affect hydrolysis of the previously proposed natural ligand of LTA4 H, Pro-Gly-Pro (PGP). This result highlights a discrepancy between the hydrolysis of more conveniently monitored chromogenic synthetic peptides typically employed in assays and endogenous peptides. The epoxide hydrolase (EH) activity of AMP was measured in vivo and the compound significantly reduced leukotriene B4 (LTB4 ) levels in a murine bacterial pneumonia model. However, AMP did not enhance survival in the murine pneumonia model over a 14-day period. A liver microsome stability assay showed metabolic stability of AMP. The results suggested that accelerated Ala-pNA cleavage is not sufficient for predicting therapeutic potential, even when the full mechanism of activation is known., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Masson SAS. All rights reserved.)- Published
- 2024
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