Stacey A Heumann

Discovery of a potent and selective aurora kinase inhibitor.

Wang Shen, Amy D. Fung, Joni W. Lam, 2008, Bioorganic & medicinal chemistry letters.

Water-soluble prodrugs of an Aurora kinase inhibitor.

Amy D. Fung, R. Mcdowell, J. Jacobs, 2009, Bioorganic & medicinal chemistry letters.

2-Aminobenzimidazoles as potent Aurora kinase inhibitors.

Amy D. Fung, T. O'Brien, W. Flanagan, 2009, Bioorganic & medicinal chemistry letters.

Diastereoselective synthesis of cyclopentapyridazinones via radical cyclization: synthetic studies toward halichlorine.

Stacey A Heumann, G. E. Keck, 2008, Organic letters.

Optimization of novel reversible Bruton's tyrosine kinase inhibitors identified using Tethering-fragment-based screens.

L. Silvian, T. Bohnert, D. Erlanson, 2019, Bioorganic & medicinal chemistry.

Utilizing structure based drug design and metabolic soft spot identification to optimize the in vitro potency and in vivo pharmacokinetic properties leading to the discovery of novel reversible Bruton's tyrosine kinase inhibitors.

Y. Liu, L. Silvian, T. Bohnert, 2021, Bioorganic & medicinal chemistry.