Institut de Chimie Moléculaire et des Matériaux d'Orsay

Laboratoire de Chimie Bioorganique et Bioinorganique - LCBB

Stéphanie Pethe

Stéphanie Pethe

Assistant professor

UMR 8182, ICMMO
Institut de Chimie Moléculaire et des Matériaux d’Orsay
Université Paris-Sud, Bât 420
91405 Orsay Cedex (France)

Tel: +33 1 69 15 47 20
Fax: +33 1 69 15 72 81

send an email


Research interest:
Subject 2

Teaching:

Publications (2006-2017):


Synthesis and in vitro antikinetoplastid activity of polyamine-hydroxybenzotriazole conjugates.
Elodie JAGU, Sébastien POMEL, Alba DIEZ-MARTINEZ, Florence RAMIANDRASOA , R. Luise KRAUTH-SIEGEL, Stéphanie PETHE, Casimir BLONSKI, Raphaël LABRUERE, Philippe M. LOISEAU
Bioorg. Med. Chem. 2017, 25, 84-90.

Design, synthesis and in vitro antikinetoplastid evaluation of N-acylated putrescine, spermidine and spermine derivatives.
Elodie JAGU, Rachid DJILLALI, Sébastien POMEL, Florence RAMIANDRASOA, Stéphanie PETHE, Raphaël LABRUERE, Philippe M. LOISEAU, Casimir BLONSKI
Bioorg. Med. Chem. Lett. 2015, 25, 207-209.


Synthesis and Biological Evaluation of Acridine Derivatives as Antimalarial Agents.
Xiao-Min YU, Florence RAMIANDRASOA, Lucie GUETZOYAN, Bruno PRADINES, Edgar QUINTINO, Danièle GADELLE, Patrick FORTERRE, Thierry CRESTEIL, Jean-Pierre MAHY, and Stéphanie PETHE
ChemMedChem 2012, 7, 587-605.

Coordination chemistry studies and peroxidase activity of a new artificial metalloenzyme built by the “Trojan horse” strategy.
Q. RAFFY, R. RICOUX, E. SANSIAUME, S. PETHE, and J.-P. MAHY
J. Mol. Catal. A: Chem. 2010, 317, 19-26.

Antimalarial acridines: Synthesis, in vitro activity against P. falciparum and interaction with hematin.
L. GUETZOYAN, X.-M. YU, F. RAMIANDRASOA, S. PETHE, C. ROGIER, B. PRADINES, T. CRESTEIL, M. PERREE-FAUVET, and J.-P. MAHY
Bioorg. Med. Chem. 2009, 17, 8032-8039.

Flavocytochrome b2 : reactivity of its flavin with molecular oxygen.
A. K. OULD BOUBACAR, S. PETHE, J.-P. MAHY, and F. LEDERER
Biochemistry 2007, 46, 13080-13088.

Molecular tongs containing amino acid mimetic fragments: new inhibitors of wild-type and mutated
HIV-1 protease dimerization.
L. BANNWARTH, A. KESSLER, S. PETHE, B. COLLINET, N. MERABET, N. BOGGETTO, S. SICSIC, M. REBOUD-RAVAUX, and S. ONGERI
J. Med. Chem. 2006, 49, 4657-4664.


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