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Bioorganic & Medicinal Chemistry Letters|March 10, 2004
Design and synthesis of indolo[2,3-a]quinolizin-7-one inhibitors of the ZipA-FtsZ interactionLee D Jennings, Ken W Foreman, Thomas S Rush, et al.
European Journal of Medicinal Chemistry|January 20, 2018
Rational approach to highly potent and selective apoptosis signal-regulating kinase 1 (ASK1) inhibitorsFrank Lovering, Paul Morgan, Christophe Allais, et al.
Bioconjugate Chemistry|December 14, 2018
Natural Product Bis-Intercalator Depsipeptides as a New Class of Payloads for Antibody-Drug ConjugatesAnokha S Ratnayake, Li-Ping Chang, L Nathan Tumey, et al.
Bioorganic & Medicinal Chemistry|September 8, 2004
Combinatorial synthesis of substituted 3-(2-indolyl)piperidines and 2-phenyl indoles as inhibitors of ZipA-FtsZ interactionLee D Jennings, Kenneth W Foreman, Thomas S Rush, et al.
ACS Nano|July 19, 2024
Portable Near-Infrared to Near-Infrared Platform for Homogeneous Quantification of Biomarkers in Complex Biological SamplesYantao Li, Xiaorui Mai, Wenming Liu, et al.
The Biochemical Journal|March 6, 2014
Selectively targeting an inactive conformation of interleukin-2-inducible T-cell kinase by allosteric inhibitorsSeungil Han, Robert M Czerwinski, Nicole L Caspers, et al.
Nature Communications|May 16, 2025
Inhibiting peptidylarginine deiminases (PAD1-4) by targeting a Ca<sup>2+</sup> dependent allosteric binding siteLeslie A Dakin, Li Xing, Justin Hall, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 2018
Delineating the role of cooperativity in the design of potent PROTACs for BTKAdelajda Zorba, Chuong Nguyen, Yingrong Xu, et al.
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