S. Yi

Identification of benzimidazole-based inhibitors of the mitogen activated kinase-5 signaling pathway.

P. Flaherty, I. Chopra, Prashi Jain, 2010, Bioorganic & medicinal chemistry letters.

Purinylpyridinylamino-based DFG-in/αC-helix-out B-Raf inhibitors: Applying mutant versus wild-type B-Raf selectivity indices for compound profiling.

D. Whittington, H. Bregman, Matthew R. Lee, 2016, Bioorganic & medicinal chemistry.

Design, synthesis, and testing of an 6-O-linked series of benzimidazole based inhibitors of CDK5/p25.

Laurent Meijer, Jeffry D Madura, L. Meijer, 2011, Bioorganic & medicinal chemistry.

Crystal structures of human glycine receptor α3 bound to a novel class of analgesic potentiators

J. Luther, H. Bregman, Xin Huang, 2016, Nature Structural &Molecular Biology.

The Discovery and Hit-to-Lead Optimization of Tricyclic Sulfonamides as Potent and Efficacious Potentiators of Glycine Receptors.

H. Bregman, Xin Huang, Liyue Huang, 2017, Journal of medicinal chemistry.

Discovery and optimization of potent and selective imidazopyridine and imidazopyridazine mTOR inhibitors.

T. Bush, A. Cheng, P. Andrews, 2012, Bioorganic & medicinal chemistry letters.

Suzuki–Miyaura Cross‐Coupling of Potassium Organoborates with 6‐Sulfonate Benzimidazoles Using Microwave Irradiation

P. Flaherty, Prashi Jain, S. Yi, 2013 .