Michael P. Hedrick

Discovery, Synthesis, and Optimization of Diarylisoxazole‐3‐carboxamides as Potent Inhibitors of the Mitochondrial Permeability Transition Pore

T. Chung, Benjamin Neuenswander, J. Aubé, 2015, ChemMedChem.

Exceptionally potent inhibitors of fatty acid amide hydrolase: the enzyme responsible for degradation of endogenous oleamide and anandamide.

D. Boger, B. Cravatt, M. Hedrick, 2000, Proceedings of the National Academy of Sciences of the United States of America.

A simple, high-resolution method for establishing DNA binding affinity and sequence selectivity.

D. Boger, M. Hedrick, B. Fink, 2001, Journal of the American Chemical Society.

10-Formyl-5,10-dideaza-acyclic-5,6,7,8-tetrahydrofolic acid (10-formyl-DDACTHF): a potent cytotoxic agent acting by selective inhibition of human GAR Tfase and the de novo purine biosynthetic pathway.

D. Boger, I. Wilson, S. Benkovic, 2002, Bioorganic & medicinal chemistry.

Discovery, Synthesis, and Optimization of Diarylisoxazole‐3‐carboxamides as Potent Inhibitors of the Mitochondrial Permeability Transition Pore

T. Chung, Benjamin Neuenswander, J. Aubé, 2015, ChemMedChem.

Total syntheses of thiocoraline and BE-22179 and assessment of their DNA binding and biological properties.

D. Boger, M. Hedrick, W. Tse, 2001, Journal of the American Chemical Society.