Kelly-Ann S. Schlegel

发表

Discovery and expanded SAR of 4,4-disubstituted quinazolin-2-ones as potent T-type calcium channel antagonists.

Steven V. Fox, James C Barrow, Cuyue Tang, 2010, Bioorganic & medicinal chemistry letters.

Identification of potent inhibitors of the sortilin-progranulin interaction.

Gregory T O'Donnell, P. Coleman, M. Ziebell, 2020, Bioorganic & medicinal chemistry letters.

Iterative Focused Screening with Biological Fingerprints Identifies Selective Asc-1 Inhibitors Distinct from Traditional High Throughput Screening.

Peter S. Kutchukian, Gregory T O'Donnell, Paul Zuck, 2017, ACS chemical biology.

Discovery of 1,4-substituted piperidines as potent and selective inhibitors of T-type calcium channels.

Steven V. Fox, S. Doran, W. Shipe, 2008, Journal of medicinal chemistry.

Pyridyl amides as potent inhibitors of T-type calcium channels.

Steven V. Fox, S. Doran, G. McGaughey, 2011, Bioorganic & medicinal chemistry letters.

Design, synthesis, and evaluation of a novel 4-aminomethyl-4-fluoropiperidine as a T-type Ca2+ channel antagonist.

Steven V. Fox, S. Doran, W. Shipe, 2008, Journal of medicinal chemistry.

Short-acting T-type calcium channel antagonists significantly modify sleep architecture in rodents.

Steven V. Fox, S. Doran, W. Zeng, 2010, ACS medicinal chemistry letters.

Positive Allosteric Interaction of Structurally Diverse T-Type Calcium Channel Antagonists

Steven V. Fox, S. Doran, J. Renger, 2009, Cell Biochemistry and Biophysics.

Discovery of 4-arylquinoline-2-carboxamides, highly potent and selective class of mGluR2 negative allosteric modulators: From HTS to activity in animal models.

J. Uslaner, V. Uebele, J. O'brien, 2020, Bioorganic & medicinal chemistry letters.