Research Assistant II

Mallory A. Maurer

Research 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.

Headshot of Mallory A. Maurer

Research Highlights

Pyridazine-Based mGlu Modulators

bioRxiv, 2025

Novel class of reversible allosteric modulators targeting mGlu1 and mGlu5 with structure-driven selectivity in cortical neuron assays.

bioRxiv

Serotonin 5-HT2 Agonists

ACS Med Chem Lett, 2024

Structure–activity study of indazole tryptamine analogs probing 5-HT2 receptor subtype selectivity.

PubMed

mGlu5 NAM Series

ACS Med Chem Lett, 2024–2025

Discovery of potent, brain-penetrant NAMs targeting mGlu5 receptors through scaffold-hopping optimization.

PubMed
Mallory Maurer in the lab
Bench work at the Warren Center for Neuroscience Drug Discovery (Vanderbilt).

Selected Publications

Selective, Reversible Chemical Modulation of mGlu1 and mGlu5 by Novel Pyridazine Derivatives
bioRxiv, 2025

Maurer M.A., Cha H., et al.

Introduces a new class of pyridazine-based allosteric modulators targeting mGlu1 and mGlu5, revealing structure-driven selectivity profiles in cortical neuron assays.

Evaluation of the Indazole Analogs of 5-MeO-DMT and Related Tryptamines as Serotonin Receptor 2 Agonists
ACS Med Chem Lett, 2024

Jayakodiarachchi N., Maurer M.A., et al.

Synthesizes and profiles indazole analogs of 5-MeO-DMT to map SAR at 5-HT2 receptors, identifying subtype-selective agonists.

Discovery of Thieno[3,2-b]pyridine-5-carboxamide and 2,3-Difluorobenzamide NAMs of mGlu5
ACS Med Chem Lett, 2025

Crocker K.E., Maurer M.A., et al.

Expands mGlu5 NAM series with new chemotypes and improved selectivity.

Development of VU6036864: A Triazolopyridine-Based High-Quality Antagonist Tool Compound of the M5 Muscarinic Receptor
J. Med. Chem., 2024

Li J., Orsi D.L., Maurer M.A., et al.

Reports discovery of a potent and selective M5 antagonist suitable as a neuroscience tool compound.

Discovery of 4-(5-Membered)Heteroarylether-6-methylpicolinamide Negative Allosteric Modulators of mGlu5
ACS Med Chem Lett, 2024

Childress E.S., Capstick R.A., Maurer M.A., et al.

Describes novel mGlu5 NAMs with optimized brain penetration and pharmacology.

Contact

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