Design, Synthesis, and Inhibitory Activity of Potent, Photoswitchable Mast Cell Activation Inhibitors

Willem A. Velema, Marco van der Toorn, Wiktor Szymanski*, Ben L. Feringa

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

42 Citations (Scopus)
668 Downloads (Pure)

Abstract

Allergic reactions affect millions of people worldwide. The need for new and effective antiallergic agents is evident, and insight into the underlying mechanisms that lead to allergic events is necessary. Herein, we report the design, synthesis, and activity of photoswitchable mast cell activation inhibitors. In mast cell degranulation assays, these inhibitors possess significantly greater potency than an original, chromone-based antiallergic agent. Furthermore, one of the photoswitchable inhibitors shows a significant difference in inhibitory activity between its two photoisomeric forms. Further optimization could ultimately lead to a photoswitchable compound suitable for studying mechanisms involved in allergic reactions in a novel manner, with activity addressable by light and with precise spatiotemporal control over events at the molecular level.

Original languageEnglish
Pages (from-to)4456-4464
Number of pages9
JournalJournal of Medicinal Chemistry
Volume56
Issue number11
DOIs
Publication statusPublished - 13-Jun-2013

Keywords

  • OPIOID RECEPTOR ANTAGONISTS
  • FC-EPSILON-RI
  • ALLERGIC RHINITIS
  • DISODIUM CROMOGLYCATE
  • AZOBENZENE PHOTOSWITCHES
  • NEDOCROMIL SODIUM
  • BIVALENT LIGANDS
  • ASTHMA DRUGS
  • CROMOLYN
  • PROTEIN

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