6-Methyl-2,4-disubstituted pyridazin-3(2H)-ones: A novel class of small-molecule agonists for formyl peptide receptors

Agostino Cilibrizzi, Mark T. Quinn, Liliya N. Kirpotina, Igor A. Schepetkin, Jeff Holderness, Richard D. Ye, Marie Josephe Rabiet, Claudio Biancalani, Nicoletta Cesari, Alessia Graziano, Claudia Vergelli, Stefano Pieretti, Vittorio Dal Piaz, Maria Paola Giovannoni

Результат исследований: Материалы для журналаСтатья

31 Цитирования (Scopus)

Аннотация

Following a ligand-based drug design approach, a potent mixed formyl peptide receptor 1 (FPR1) and formyl peptide receptor-like 1 (FPRL1) agonist (14a) and a potent and specific FPRL1 agonist (14x) were identified. These compounds belong to a large series of pyridazin-3(2H)-one derivatives substituted with a methyl group at position 6 and a methoxy benzyl at position 4. At position 2, an acetamide side chain is essential for activity. Likewise, the presence of lipophilic and/or electronegative substituents in the position para to the aryl group at the end of the chain plays a critical role for activity. Affinity forFPR1 receptors was evaluated by measuring intracellular calcium flux in HL-60 cells transfected with FPR1, FPRL1, and FPRL2. Agonists were able to activate intracellular calcium mobilization and chemotaxis in human neutrophils. Themost potent chemotactic agent (EC50 =0.6 μM) was the mixed FPR/FPRL1 agonist 14h.

Язык оригиналаАнглийский
Страницы (с-по)5044-5057
Число страниц14
ЖурналJournal of Medicinal Chemistry
Том52
Номер выпуска16
DOI
СостояниеОпубликовано - 27 авг 2009
Опубликовано для внешнего пользованияДа

ASJC Scopus subject areas

  • Molecular Medicine
  • Drug Discovery

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  • Цитировать

    Cilibrizzi, A., Quinn, M. T., Kirpotina, L. N., Schepetkin, I. A., Holderness, J., Ye, R. D., Rabiet, M. J., Biancalani, C., Cesari, N., Graziano, A., Vergelli, C., Pieretti, S., Dal Piaz, V., & Giovannoni, M. P. (2009). 6-Methyl-2,4-disubstituted pyridazin-3(2H)-ones: A novel class of small-molecule agonists for formyl peptide receptors. Journal of Medicinal Chemistry, 52(16), 5044-5057. https://doi.org/10.1021/jm900592h