1. Academic Validation
  2. Novel 1‑Phenyl-2,3-dihydroquinazolin-4(1H)-one Derivatives as Nav 1.8 Voltage-Gated Sodium Channels Inhibitors

Novel 1‑Phenyl-2,3-dihydroquinazolin-4(1H)-one Derivatives as Nav 1.8 Voltage-Gated Sodium Channels Inhibitors

  • ACS Med Chem Lett. 2026 Apr 22;17(5):1028-1030. doi: 10.1021/acsmedchemlett.6c00189.
Ruihu Song 1 Steven H Liang 1 2
Affiliations

Affiliations

  • 1 Department of Radiology and Imaging Sciences, Emory University, 1364 Clifton Road, Atlanta, Georgia 30322, United States.
  • 2 Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia 30332, United States.
Abstract

This highlight outlines the development of novel substituted 1-phenyl-2,3-dihydroquinazolin-4-(1H)-one derivatives as potential inhibitor candidates for Nav 1.8 voltage-gated sodium channels (Nav 1.8), which is upregulated or activated to transmit nociceptive signaling in a range of pain-related disorders. The invention includes details on preparation methods, biological activity assays, and pharmaceutical compositions.

Figures
Products