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Jean-Michel Luccarini

41

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Abstract B14: Discovery of YAP-TEAD protein-protein interaction inhibitors (PPI) for treating malignant pleural mesothelioma (MPM)

2020 Molecular Cancer Research
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Odiparcil is a promising substrate reduction therapy in MPS VI murine model

2018 Molecular Genetics and Metabolism
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Design, Synthesis, and Evaluation of a Novel Series of Indole Sulfonamide Peroxisome Proliferator Activated Receptor (PPAR) α/γ/δ Triple Activators: Discovery of Lanifibranor, a New Antifibrotic Clinical Candidate

2018 Journal of Medicinal Chemistry
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IVA337, a pan-ppar agonist, reduces non-alcoholic steatohepatitis feature and inhibits the inflammasome in murin models of non-alcoholic steatohepatitis

2017 Journal of Hepatology
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The New Generation Pan-Ppar Agonist Iva337 Protects the Liver from Metabolic Disorders and Fibrosis

2016 Journal of Hepatology
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L’agoniste pan-PPAR IVA337 est efficace pour la prévention de la fibrose pulmonaire et de l’hypertension pulmonaire expérimentales

2016 Revue du Rhumatisme
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Pan PPAR agonist IVA337 is effective in prevention and treatment of experimental skin fibrosis

2015 Annals of the Rheumatic Diseases
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From bradykinin B2 receptor antagonists to orally active and selective bradykinin B1 receptor antagonists.

2012 Journal of Medicinal Chemistry
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Benzenesulfonamide derivatives, process for their preparation and their use for the treatment of pain

2004
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Derives du benzenesulfonamide, leur procede de preparation et leur utilisation de la douleur

2004
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