Targeting Acidic Mammalian chitinase Is Effective in Animal Model of Asthma

Archive ouverte

Mazur, Marzena | Olczak, Jacek | Olejniczak, Sylwia | Koralewski, Robret | Czestkowski, Wocjiech | Jedrzejczak, Anna | Golab, Jakub | Dzwonek, Karolina | Dymek, Barbara | Sklepkiewicz, Piotr | Zagozdzon, Agnieszka | Noonan, Tom | Mahboubi, Keyvan | Conway, Bruce | Sheeler, Ryan | Beckett, Paul | Hungerford, William | Podjarny, Alberto | Mitschler, André | Cousido-Siah, Alexandra | Fadel, Firas | Golebiowski, Adam

Edité par CCSD ; American Chemical Society -

This article highlights our work toward the identification of a potent, selective, and efficacious acidic mammalian chitinase (AMCase) inhibitor. Rational design, guided by X-ray analysis of several inhibitors bound to human chitotriosidase (hCHIT1), led to the identification of compound 7f as a highly potent AMCase inhibitor (IC50 values of 14 and 19 nM against human and mouse enzyme, respectively) and selective (>150x against mCHIT1) with very good PK properties. This compound dosed once daily at 30 mg/kg po showed significant anti-inflammatory efficacy in HDM-induced allergic airway inflammation in mice, reducing inflammatory cell influx in the BALF and total IgE concentration in plasma, which correlated with decrease of chitinolytic activity. Therapeutic efficacy of compound 7f in the clinically relevant aeroallergen-induced acute asthma model in mice provides a rationale for developing AMCase inhibitor for the treatment of asthma.

Consulter en ligne

Suggestions

Du même auteur

Synthesis of quaternary α-amino acid-based arginase inhibitors via the Ugi reaction

Archive ouverte | Golebiowski, Adam | CCSD

International audience

Discovery of (R)-2-amino-6-borono-2-(2-(piperidin-1-yl)ethyl)hexanoic acid and congeners as highly potent inhibitors of human arginases I and II for treatment of myocardial reperfusion injury

Archive ouverte | van Zandt, Michael C. | CCSD

Recent efforts to identify treatments for myocardial ischemia reperfusion injury have resulted in the discovery of a novel series of highly potent alpha,alpha-disubstituted amino acid-based arginase inhibitors. The lead candidate,...

2-Substituted-2-amino-6-boronohexanoic acids as arginase inhibitors

Archive ouverte | Golebiowski, Adam | CCSD

International audience

Chargement des enrichissements...