Aaron D. Krabill
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
Publications
15
Citations
282
Est. group size
~8
Recurring co-author estimate
Active years
7
Publishing since 2019
Aaron D. Krabill's research focuses on designing small-molecule drugs that target specific enzymes involved in disease, particularly protein tyrosine phosphatases (enzymes that remove phosphate groups from proteins, affecting cell signaling) and deubiquitinases (enzymes that remove ubiquitin tags used to mark proteins for degradation or regulation). Much of this work involves creating covalent inhibitors—molecules that form a permanent chemical bond with their target—as potential treatments for cancer, neurodegenerative disease, and antibiotic-resistant bacterial infections. The work combines medicinal chemistry (drug design) with biochemistry to characterize how these inhibitors work at a molecular level.
Publication output has been modest and somewhat uneven over the last decade, with a recent increase in activity in 2024-2025 following a gap in 2022.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Discovery of a First‐in‐Class Covalent Allosteric SHP1 Inhibitor with Immunotherapeutic Activity
Angewandte Chemie International Edition · 2025
- Discovery and Evaluation of Active Site-Directed, Potent, and Selective Sulfophenyl Acetic Amide-Based Inhibitors for the Laforin Phosphatase
Journal of Medicinal Chemistry · 2025
- Discovery of a First‐in‐Class Covalent Allosteric SHP1 Inhibitor with Immunotherapeutic Activity
Angewandte Chemie · 2025
- Covalent Fragment Screening and Optimization Identifies the Chloroacetohydrazide Scaffold as Inhibitors for Ubiquitin C-terminal Hydrolase L1
Journal of Medicinal Chemistry · 2024
- Natural product-inspired molecules for covalent inhibition of SHP2 tyrosine phosphatase
Tetrahedron · 2024
- Altered Protein Dynamics and a More Reactive Catalytic Cysteine in a Neurodegeneration-associated UCHL1 Mutant
Journal of Molecular Biology · 2024
- Abstract 1973: Discovery of the first-in-class SHP1 covalent inhibitor for cancer immunotherapy
Cancer Research · 2024
- High-Throughput Discovery and Characterization of Covalent Inhibitors for Protein Tyrosine Phosphatases
Methods in molecular biology · 2023
- Functional interrogation and therapeutic targeting of protein tyrosine phosphatases
Biochemical Society Transactions · 2021
- Optimization and Anti-Cancer Properties of Fluoromethylketones as Covalent Inhibitors for Ubiquitin C-Terminal Hydrolase L1
Molecules · 2021
- Optimization of Acetazolamide-Based Scaffold as Potent Inhibitors of Vancomycin-Resistant <i>Enterococcus</i>
Journal of Medicinal Chemistry · 2020
- Development of Ubiquitin Variants with Selectivity for Ubiquitin C-Terminal Hydrolase Deubiquitinases
Biochemistry · 2020
- Corrigendum: Ubiquitin C‐Terminal Hydrolase L1: Biochemical and Cellular Characterization of a Covalent Cyanopyrrolidine‐Based Inhibitor
ChemBioChem · 2020
- Journal of Medicinal Chemistry×3
- ChemBioChem×2
- ACS Infectious Diseases×1
- Biochemical Society Transactions×1
- Molecules×1
- Rishi Patel
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Christine S. Muli
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Darci J. Trader
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Jiaxing Miao
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Jing Zhao
Biochemistry, Genetics and Molecular Biology · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 20, 2026.
Claim or correct this profile