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12. Discovery of dihydroisoquinolinone derivatives as novel inhibitors of the p53–MDM2 interaction with a distinct binding mode. Issue 17 (1st September 2015)

13. Front Cover: Structural States of Hdm2 and HdmX: X‐ray Elucidation of Adaptations and Binding Interactions for Different Chemical Compound Classes (ChemMedChem 14/2019). (17th July 2019)

14. Front Cover: The First Class of Small Molecules Potently Disrupting the YAP‐TEAD Interaction by Direct Competition (ChemMedChem 19/2022). (6th October 2022)

15. Identification and optimisation of 4, 5-dihydrobenzo[1, 2-d:3, 4-d]bisthiazole and 4, 5-dihydrothiazolo[4, 5-h]quinazoline series of selective phosphatidylinositol-3 kinase alpha inhibitors. Issue 17 (1st September 2015)

16. Identification and optimisation of a 4′, 5-bisthiazole series of selective phosphatidylinositol-3 kinase alpha inhibitors. Issue 17 (1st September 2015)

18. Identification of FAM181A and FAM181B as new interactors with the TEAD transcription factors. (20th November 2019)

19. In vitro and in vivo characterization of a novel, highly potent p53-MDM2 inhibitor. Issue 20 (1st November 2018)

20. Molecular and structural characterization of a TEAD mutation at the origin of Sveinsson's chorioretinal atrophy. (11th April 2019)