Live virtual event
May 5, 2025 | 2�3 PM PT
60 minutes
Pasadena, CA
Multitopic
Work in the Hopkins Laboratory centers around the synthesis and optimization of novel chemical tool compounds aimed at tackling unmet medical needs. This talk will cover two projects in my lab: 1. Characterization of novel GIRK1/2 activators for the treatment of neuropathic pain, and 2. The synthesis, optimization and biological characterization of a series of sigma 1 modulators derived from dopamine 4 antagonists and their use in animal models of pain. GIRK1/2 activators are a class of compounds that can modulate G-protein-coupled inwardly rectifying potassium channels, which are involved in pain signaling pathways.
By enhancing GIRK channel activity, these activators have shown potential in reducing pain perception and providing analgesic effects in preclinical animal models. The work presented herein outlines the ongoing structure-activity relationship (SAR) studies centered around a potent, efficacious, and selective positive allosteric modulators (PAM) of the GIRK1/2 channel. Sigma 1 antagonists have gained attention for their potential to modulate pain by blocking the sigma-1 receptor, which is involved in various cellular processes, including pain transmission. Preclinical studies suggest that these antagonists may reduce nociceptive signaling, offering a novel approach to pain management. In the second part, he describes his efforts at the identification of novel dopamine 4 receptor antagonists and how that effort morphed into the discovery of potent and selective sigma 1 modulators.
Speaker
Event Location- 2700 East Foothills Blvd, # 209, Pasadena, CA 91107
Keep learning. Excel in your career.
Choose from more than 200 courses in seven different categories, taught by experts in the chemistry community, online and in person.