Jeanine E. Price

发表

Chemical scaffold recycling: Structure-guided conversion of an HIV integrase inhibitor into a potent influenza virus RNA-dependent RNA polymerase inhibitor designed to minimize resistance potential.

R. Webby, R. DuBois, Jeremy C. Jones, 2022, European journal of medicinal chemistry.

Synthesis of an aryloxy oxo pyrimidinone library that displays ALK-selective inhibition.

S. Morris, T. Webb, Q. Jiang, 2011, Bioorganic & medicinal chemistry letters.

Evaluation of Diarylureas for Activity Against Plasmodium falciparum.

J. Derisi, R. Guy, J. L. Weisman, 2010, ACS medicinal chemistry letters.

Structure-activity relationships of substituted 1-pyridyl-2-phenyl-1,2-ethanediones: potent, selective carboxylesterase inhibitors.

Taosheng Chen, David C. Bouck, P. Potter, 2010, Journal of medicinal chemistry.

Identification of Potent, Selective, and Orally Bioavailable Small-Molecule GSPT1/2 Degraders from a Focused Library of Cereblon Modulators

M. Roussel, C. Mullighan, M. Fischer, 2021, Journal of Medicinal Chemistry.

2-Substituted-4,5-dihydroxypyrimidine-6-carboxamide antiviral targeted libraries.

T. Webb, V. Boyd, Parimala Hanumesh, 2009, Journal of combinatorial chemistry.

Efficient synthesis of pyrazolopyrimidine libraries.

T. Webb, P. J. Slavish, Parimala Hanumesh, 2010, Journal of combinatorial chemistry.

Bromodomain-Selective BET Inhibitors Are Potent Antitumor Agents against MYC-Driven Pediatric Cancer

M. Roussel, Taosheng Chen, A. Shelat, 2020, Cancer Research.

Structure-activity relationships of substituted 1-pyridyl-2-phenyl-1,2-ethanediones: potent, selective carboxylesterase inhibitors.

Taosheng Chen, David C. Bouck, P. Potter, 2010, Journal of medicinal chemistry.