Pyridazine-Based mGlu Modulators
Novel class of reversible allosteric modulators targeting mGlu1 and mGlu5 with structure-driven selectivity in cortical neuron assays.
bioRxivResearch Assistant II at the Cha Lab, exploring chemical biology strategies to study neural GPCRs and neuromodulatory systems. Formerly at Vanderbilt's Warren Center for Neuroscience Drug Discovery. Applying to biomedical engineering PhD programs in Fall 2025.
Novel class of reversible allosteric modulators targeting mGlu1 and mGlu5 with structure-driven selectivity in cortical neuron assays.
bioRxivStructure–activity study of indazole tryptamine analogs probing 5-HT2 receptor subtype selectivity.
PubMedDiscovery of potent, brain-penetrant NAMs targeting mGlu5 receptors through scaffold-hopping optimization.
PubMed
Introduces a new class of pyridazine-based allosteric modulators targeting mGlu1 and mGlu5, revealing structure-driven selectivity profiles in cortical neuron assays.
Synthesizes and profiles indazole analogs of 5-MeO-DMT to map SAR at 5-HT2 receptors, identifying subtype-selective agonists.
Expands mGlu5 NAM series with new chemotypes and improved selectivity.
Reports discovery of a potent and selective M5 antagonist suitable as a neuroscience tool compound.
Describes novel mGlu5 NAMs with optimized brain penetration and pharmacology.
LinkedIn: linkedin.com/in/mallory-maurer-25b1a3229
Current Role: Research Assistant II at the Cha Lab, Chemical Biology & GPCR Research
Previous: Warren Center for Neuroscience Drug Discovery, Vanderbilt University
Status: Applying to PhD programs in Fall 2025