Publications by authors named "Michele Reboud-Ravaux"

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[Protein induced proximity and targeted degradations by new degraders: concepts, developments, challenges for clinical applications].
Michèle Reboud-Ravaux

Biol Aujourdhui· July 2024

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[Not Available].
Michèle Reboud-Ravaux

Biol Aujourdhui· March 2022

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The HIV-1 Nucleocapsid Regulates Its Own Condensation by Phase-Separated Activity-Enhancing Sequestration of the Viral Protease during Maturation.
Sébastien Lyonnais, S Kashif Sadiq, Cristina Lorca-Oró, Laure Dufau, Sara Nieto-Marquez, Michèle Reboud-Ravaux

Viruses· November 2021

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[The proteasome - structural aspects and inhibitors: a second life for a validated drug target].
Michèle Reboud-Ravaux

Biol Aujourdhui· October 2021

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[Induced degradation of proteins by PROTACs and other strategies: towards promising drugs].
Michèle Reboud-Ravaux

Biol Aujourdhui· August 2021

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Structural Studies on the Inhibitory Binding Mode of Aromatic Coumarinic Esters to Human Kallikrein-Related Peptidase 7.
Stefanie Hanke, Catherine A Tindall, Jan Pippel, David Ulbricht, Bernard Pirotte, Michèle Reboud-Ravaux

J Med Chem· June 2020

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Insights into the activity control of the kallikrein-related peptidase 6: small-molecule modulators and allosterism.
Feryel Soualmia, Elodie Bosc, Sabrina Aït Amiri, Dirk Stratmann, Viktor Magdolen, Michèle Reboud-Ravaux

Biol Chem· September 2018

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Structure-based design of human immuno- and constitutive proteasomes inhibitors.
Nicolas Richy, Daad Sarraf, Xavier Maréchal, Naëla Janmamode, Rémy Le Guével, Michèle Reboud-Ravaux

Eur J Med Chem· February 2018

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Piperlongumine and some of its analogs inhibit selectively the human immunoproteasome over the constitutive proteasome.
Elodie Bosc, Jhennifer Nastri, Valérie Lefort, Marilia Valli, Fernando Contiguiba, Michèle Reboud-Ravaux

Biochem Biophys Res Commun· February 2018

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Phenoxypropanolamine derivatives as selective inhibitors of the 20S proteasome β1 and β5 subunits.
Anna A Hovhannisyan, The Hien Pham, Dominique Bouvier, Xiao Tan, SiAmmar Touhar, Michèle Reboud-Ravaux

Bioorg Med Chem Lett· December 2017

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Blockade of the malignant phenotype by β-subunit selective noncovalent inhibition of immuno- and constitutive proteasomes.
Bruno O Villoutreix, Abdel-Majid Khatib, Yan Cheng, Maria A Miteva, Xavier Maréchal, Michèle Reboud-Ravaux

Oncotarget· February 2017

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Identification of a β1/β2-specific sulfonamide proteasome ligand by crystallographic screening.
Philipp Beck, Michèle Reboud-Ravaux, Michael Groll

Angew Chem Int Ed Engl· September 2015

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Bisbenzimidazole derivatives as potent inhibitors of the trypsin-like sites of the immunoproteasome core particle.
Olga N Koroleva, The Hien Pham, Dominique Bouvier, Laure Dufau, Lixian Qin, Michèle Reboud-Ravaux

Biochimie· January 2015

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Jatrophidin I, a cyclic peptide from Brazilian Jatropha curcas L.: isolation, characterization, conformational studies and biological activity.
Wanessa F Altei, Douglas G Picchi, Barbara M Abissi, Guilherme M Giesel, Otavio Flausino, Michèle Reboud-Ravaux

Phytochemistry· November 2014

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Noncovalent fluorescent probes of human immuno- and constitutive proteasomes.
Audrey Desvergne, Yan Cheng, Sophie Grosay-Gaudrel, Xavier Maréchal, Michèle Reboud-Ravaux

J Med Chem· November 2014

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α- and β-hydrazino acid-based pseudopeptides inhibit the chymotrypsin-like activity of the eukaryotic 20S proteasome.
Andrea Bordessa, Massaba Keita, Xavier Maréchal, Lucia Formicola, Nathalie Lagarde, Michèle Reboud-Ravaux

Eur J Med Chem· September 2014

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Identification by in silico and in vitro screenings of small organic molecules acting as reversible inhibitors of kallikreins.
Xiao Tan, Claudia Bertonati, Lixian Qin, Laetitia Furio, Chahrazade El Amri, Michèle Reboud-Ravaux

Eur J Med Chem· September 2014

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New C(4)- and C(1)-derivatives of furo[3,4-c]pyridine-3-ones and related compounds: evidence for site-specific inhibition of the constitutive proteasome and its immunoisoform.
Anna Hovhannisyan, The Hien Pham, Dominique Bouvier, Alexander Piroyan, Laure Dufau, Michèle Reboud-Ravaux

Bioorg Med Chem Lett· March 2014

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1,2,4-Triazole derivatives as transient inactivators of kallikreins involved in skin diseases.
Xiao Tan, Laetitia Furio, Michèle Reboud-Ravaux, Bruno O Villoutreix, Alain Hovnanian

Bioorg Med Chem Lett· August 2013

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C1 and N5 derivatives of cerpegin: synthesis of a new series based on structure-activity relationships to optimize their inhibitory effect on 20S proteasome.
Anna Hovhannisyan, The Hien Pham, Dominique Bouvier, Lixian Qin, Gagik Melikyan, Michèle Reboud-Ravaux

Bioorg Med Chem Lett· May 2013

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Dimerized linear mimics of a natural cyclopeptide (TMC-95A) are potent noncovalent inhibitors of the eukaryotic 20S proteasome.
Audrey Desvergne, Emilie Genin, Xavier Maréchal, Nerea Gallastegui, Laure Dufau, Michèle Reboud-Ravaux

J Med Chem· April 2013

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Carbonylhydrazide-based molecular tongs inhibit wild-type and mutated HIV-1 protease dimerization.
Laure Dufau, Ana Sofia Marques Ressurreição, Roberto Fanelli, Nadjib Kihal, Anamaria Vidu, Michèle Reboud-Ravaux

J Med Chem· August 2012

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Noncovalent inhibition of 20S proteasome by pegylated dimerized inhibitors.
Xavier Maréchal, Anaïs Pujol, Nicolas Richy, Emilie Genin, Nicolas Basse, Michèle Reboud-Ravaux

Eur J Med Chem· June 2012

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A new series of N5 derivatives of the 1,1,5-trimethyl furo[3,4-c]pyridine-3,4-dione (cerpegin) selectively inhibits the post-acid activity of mammalian 20S proteasomes.
The Hien Pham, Anna Hovhannisyan, Dominique Bouvier, Lei Tian, Michèle Reboud-Ravaux

Bioorg Med Chem Lett· June 2012

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