Christophe Morice

发表

Toward the identification of viral cap-methyltransferase inhibitors by fluorescence screening assay

B. Coutard, J. Contreras, E. Decroly, 2017, Antiviral Research.

Structural, Magnetic, and Dynamic Characterization of the (dxz,dyz)4(dxy)1 Ground-State Low-Spin Iron(III) Tetraphenylporphyrinate Complex [(p-TTP)Fe(2,6-XylylNC)2]CF3SO3

F. Walker, V. Schünemann, L. Toupet, 2000 .

Chryso-lactams:Gold(I) derivatives of ampicillin with specific activity against Gram-positive pathogens.

J. Contreras, I. Schalk, G. L. Mislin, 2020, Bioorganic & medicinal chemistry letters.

Porphyrin Derivatives Inhibit the Interaction between Receptor Activator of NF‐κB and Its Ligand

O. Chaloin, Mélanie Chypre, C. Mueller, 2017, ChemMedChem.

N-Acetyl-3-aminopyrazoles block the non-canonical NF-kB cascade by selectively inhibiting NIK.

M. Kubbutat, J. Contreras, S. Al-Karadaghi, 2018, MedChemComm.

Discovery, Structure-Activity Relationship, and Antiparkinsonian Effect of a Potent and Brain-Penetrant Chemical Series of Positive Allosteric Modulators of Metabotropic Glutamate Receptor 4.

F. Conquet, D. Charvin, G. Hédou, 2017, Journal of medicinal chemistry.

Synthesis and Characterization of Low-Spin Bis(amino ester) Iron(III) Porphyrin Complexes.

G. Simonneaux, Paul le Maux, Christophe Morice, 1998, Inorganic chemistry.

Chapter 9 – Ring Transformations

C. Wermuth, Christophe Morice, 2008 .

Chapter 16 – Ring Transformations

C. Wermuth, Christophe Morice, 2008 .

1,2,3-Triazole-gold(I)-triethylposphine derivatives active against resistant Gram-positive pathogens.

J. Contreras, I. Schalk, G. L. Mislin, 2021, Bioorganic & medicinal chemistry letters.

Oxidation of amino esters to imine complexes with chiral high-valent oxoruthenium porphyrins

C. Moinet, G. Simonneaux, P. L. Maux, 1998 .

Chiral recognition of amino esters by ruthenium porphyrin complexes and crystal structure of {5,10,15,20-tetrakis[o-(3,3,3-trifluoro-2-methoxy-2-phenylpropanoylamino)phenyl]porphyrin}bis(L-valine methyl ester)ruthenium(II) (α,α,β,β isomer)

L. Toupet, G. Simonneaux, P. L. Maux, 1998 .

Novel allenylidene alkynyl and ammonia alkynyl metal complexes via selective synthesis of mono and bis alkynyl ruthenium(II) complexes; crystal structure of trans-[Ru(NH3)(CCPh)(Ph2PCH2CH2PPh2)2]PF6

V. Cadierno, L. Toupet, Pierre Haquette, 1994 .

Approved drugs screening against the nsP1 capping enzyme of Venezuelan equine encephalitis virus using an immuno‐based assay

B. Coutard, J. Contreras, E. Decroly, 2019, Antiviral research.

Synthesis of constrained arylpiperidines using intramolecular Heck or radical reactions

C. Wermuth, K. Briner, A. Mann, 2001 .

Discovery of BNC375, a Potent, Selective, and Orally Available Type I Positive Allosteric Modulator of α7 nAChRs.

L. Schaeffer, A. Harvey, Belinda C. Huff, 2019, ACS medicinal chemistry letters.

Fragment pharmacophore-based in silico screening: a powerful approach for efficient lead discovery

Maria Dalko-Csiba, Thierry Langer, Roger Rozot, 2016 .

Moderately lipophilic 2-(Het)aryl-6-dithioacetals, 2-phenyl-1,4-benzodioxane-6-dithioacetals and 2-phenylbenzofuran-5-dithioacetals: Synthesis and primary evaluation as potential antidiabetic AMPK-activators.

J. Contreras, A. Gruzman, S. Sasson, 2023, Bioorganic & medicinal chemistry.

4-Hydroxy-N-[3,5-bis(trifluoromethyl)phenyl]-1,2,5-thiadiazole-3-carboxamide: a novel inhibitor of the canonical NF-κB cascade.

M. Kubbutat, J. Contreras, S. Al-Karadaghi, 2017, MedChemComm.