Li-Hsing Chen

发表

Structure-activity relationship studies of a novel series of anthrax lethal factor inhibitors.

M. Pellecchia, E. Barile, Jun Wei, 2009, Bioorganic & medicinal chemistry.

Targeting Metalloproteins by Fragment‐Based Lead Discovery

Seth M. Cohen, A. Strongin, A. Osterman, 2011, Chemical biology & drug design.

Identification of a new JNK inhibitor targeting the JNK-JIP interaction site

Maurizio Pellecchia, Giovanni Solinas, Michael Karin, 2008, Proceedings of the National Academy of Sciences.

Development of paramagnetic probes for molecular recognition studies in protein kinases.

M. Pellecchia, S. De, J. Stebbins, 2008, Journal of medicinal chemistry.

A Novel Pharmacophore Model for the Design of Anthrax Lethal Factor Inhibitors

M. Pellecchia, Jun Wei, Sherida L. Johnson, 2010, Chemical biology & drug design.

A high-throughput screening approach to anthrax lethal factor inhibition.

M. Pellecchia, Sherida L. Johnson, Li-Hsing Chen, 2006, Bioorganic chemistry.

Design, synthesis, and structure-activity relationship of substrate competitive, selective, and in vivo active triazole and thiadiazole inhibitors of the c-Jun N-terminal kinase.

Elisa Barile, Maurizio Pellecchia, Hongbin Yuan, 2009, Journal of medicinal chemistry.

Chelator Fragment Libraries for Targeting Metalloproteinases

Seth M. Cohen, M. Pellecchia, Sherida L. Johnson, 2010, ChemMedChem.

Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitors.

M. Pellecchia, E. Barile, S. De, 2010, Bioorganic & medicinal chemistry.

Design and characterization of a potent and selective dual ATP- and substrate-competitive subnanomolar bidentate c-Jun N-terminal kinase (JNK) inhibitor.

M. Karin, M. Pellecchia, P. Pavlícková, 2011, Journal of Medicinal Chemistry.

Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitors.

M. Pellecchia, E. Barile, S. De, 2009, Bioorganic & medicinal chemistry.

Rhodanine Derivatives as Selective Protease Inhibitors Against Bacterial Toxins

A. Strongin, M. Pellecchia, Naomi J H Cotton, 2008, Chemical biology & drug design.

Design and characterization of a potent and selective dual ATP- and substrate-competitive subnanomolar bidentate c-Jun N-terminal kinase (JNK) inhibitor.

M. Karin, M. Pellecchia, P. Pavlícková, 2011, Journal of medicinal chemistry.