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14 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Design, Synthesis, and Biological Evaluation of Novel Activators of Human Caseinolytic Protease P with a Pyrazololactam Scaffold.EBI
China Pharmaceutical University
Harnessing the Magic Methyl Effect: Discovery of CLPP-2068 as a Novel HsClpP Activator for the Treatment of Diffuse Large B-Cell Lymphoma.EBI
Shanghai Institute of Materia Medica
ONC201-Derived Tetrahydropyridopyrimidindiones as Powerful ClpP Protease Activators to Tackle Diffuse Midline Glioma.EBI
University of Bari Aldo Moro
Structure-Guided Development of ClpP Agonists with Potent Therapeutic Activities against Staphylococcus aureus Infection.EBI
Shanghai Institute of Materia Medica
NVP-BHG712: Effects of Regioisomers on the Affinity and Selectivity toward the EPHrin Family.EBI
Johann Wolfgang Goethe University
Assessment of the structure-activity relationship and antileukemic activity of diacylpyramide compounds as human ClpP agonists.EBI
University of Chinese Academy of Sciences
Discovery of Dehydrogenated Imipridone Derivatives as Activators of Human Caseinolytic Protease P.EBI
China Pharmaceutical University
Rational Design of a Novel Class of Human ClpP Agonists through a Ring-Opening Strategy with Enhanced Antileukemia Activity.EBI
Sichuan University
Discovery of a Novel Series of Homo sapiens Caseinolytic Protease P Agonists for Colorectal Adenocarcinoma Treatment via ATF3-Dependent Integrated Stress Response.EBI
Sichuan University
Discovery of 5-(Piperidin-4-yl)-1,2,4-oxadiazole Derivatives as a New Class of Human Caseinolytic Protease P Agonists for the Treatment of Hepatocellular Carcinoma.EBI
Sichuan University
The evolution of small molecule enzyme activators.EBI
University of Nebraska
Discovery of a Novel Series of Imipridone Compounds as EBI
Sichuan University
Proteases and Their Modulators in Cancer Therapy: Challenges and Opportunities.EBI
Sichuan University
De Novo Design of Boron-Based Peptidomimetics as Potent Inhibitors of Human ClpP in the Presence of Human ClpX.EBI
University of Toronto