J. Paris

发表

Carbazolequinone induction of caspase-dependent cell death in Src-overexpressing cells.

G. Gillet, A. Aouacheria, B. Néel, 2002, Biochemical pharmacology.

Molecular modeling of hen egg lysozyme HEL[52-61] peptide binding to I-Ak MHC class II molecule.

P. Carrupt, B. Testa, D. Gerlier, 1998, International immunology.

New organometallic approach to derivatives of α-substituted statines from N,N-dibenzylaminoaldehydes

B. Cazes, J. Paris, N. Goff, 2002 .

Critical residue combinations dictate peptide presentation by MHC class II molecules

C. Rabourdin-Combe, D. Gerlier, Jean‐François Hernandez, 1994, Peptides.

An accessory peptide binding site with allosteric effect on the formation of peptide-MHC-II complexes?

D. Gerlier, J. Paris, M. Trescol-Biémont, 1998, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Design of peptide competitors for the MHC class II molecule I-Ak

C. Rabourdin-Combe, D. Gerlier, Jean‐François Hernandez, 1993 .

First Application of the Dakin-West Reaction to Fmoc Chemistry: Synthesis of the ketomethylene tripeptide Fmoc-Nα-Asp(tBu)-(R,S)Tyr(tBu)Ψ(CO-CH2)Gly-OH

J. Casimir, J. Paris, L. Ettouati, 1995 .

Inhibition of P-glycoprotein-mediated multidrug efflux by aminomethylene and ketomethylene analogs of reversins.

C. Dumontet, J. Paris, D. Guilet, 2006, Bioorganic & medicinal chemistry letters.

Conformational restriction of the Tyr53 side-chain in the decapeptide HE.

C. Rabourdin-Combe, D. Gerlier, H. Dumortier, 2000, The journal of peptide research : official journal of the American Peptide Society.

AROYLSPIROBUTENOLIDES AND THEIR REDUCED DERIVATIVES: NEW ANALGESIC COMPOUNDS

J. Paris, M. Payard,, J. Bastide, 1983 .

Synthesis of propargylic alcohols and biological effects on Echinococcus multilocularis metacestodes.

C. Gabrion, I. Delabre, J. Paris, 1993, Journal of pharmaceutical sciences.

A convenient method for the synthesis of norstatine derivatives from N-Fmoc or N-Boc amino acids

J. Paris, Saïd Kourtal, 1996, Letters in Peptide Science.

Formation of bis (Fmoc-amino ethyl)-N-glycine derivatives by reductive amination of Fmoc-amino aldehydes with NaBH3CN

N. Walchshofer, J. Paris, J. Salvi, 1994 .

Pharmacokinetics of an anthelmintic potential prodrug of a new benzimidazole in gerbil, mouse and sheep

N. Walchshofer, J. Paris, P. Delatour, 1991 .

Anthelmintic activity of 3,6-dibenzyl-2,5-dioxopiperazine, cyclo(L-Phe-L-Phe)

F. Garnier, N. Walchshofer, J. Paris, 1997, Amino Acids.

Biological effects of a dipeptide methyl ester on Echinococcus multilocularis metacestodes in vivo

N. Walchshofer, J. Paris, A. Pétavy, 1993 .

In vivo and in vitro effects of methacrylanilides and acetylcarboxanilide on alkaline phosphatase activity of Echinococcus multilocularis metacestodes

J. Paris, A. Pétavy, P. Audin, 1992 .

In vivo morphological damage induced by a new benzimidazole prodrug in Echinococcus multilocularis metacestodes.

N. Walchshofer, J. Paris, A. Pétavy, 1990, Journal of pharmaceutical sciences.

Echinococcus multilocularis metacestodes: biochemical and ultrastructural investigations on the effect of isatin (2-3 indoline dione) in vivo.

C. Gabrion, J. Paris, A. Pétavy, 1989, The Journal of antimicrobial chemotherapy.

New application of the Julia olefination for the synthesis of Tyr-Gly E-alkene and carba isostere pseudopeptides

J. Paris, L. Ettouati, Cécile Charrier, 1999 .

Synthesis of 2-methyl-5-amino-4-oxo-3-sulfonyl esters as precursors of pseudodipeptides

J. Paris, L. Ettouati, D. Severi, 2006, Letters in Peptide Science.

An efficient synthesis of anhydrides of 2-monosubstituted succinic acid monoesters and their application to the Dakin-West reaction: Isolation of some 5-succinyloxyoxazole intermediates

J. Casimir, J. Paris, L. Ettouati, 2006, Letters in Peptide Science.

Interaction of synthetic compounds with UTP-D-glucose 1-phosphate uridylyl transferase of Echinococcus multilocularis metacestodes.

J. Paris, A. Pétavy, P. Audin, 1988, Biochemical pharmacology.

Potent and fully noncompetitive peptidomimetic inhibitor of multidrug resistance P-glycoprotein.

A. di Pietro, C. Dumontet, P. Falson, 2010, Journal of medicinal chemistry.

Synthesis, biological activity and molecular modelling of the 53-54 ketomethylene analogue of HEL(52-61)

P. Carrupt, B. Testa, D. Gerlier, 1998 .

Synthesis and antiproliferative activity of [2-(phthaloylamino)alkyl]triphenyl phosphonium derivatives against K562 cell line

C. Trentesaux, N. Walchshofer, J. Paris, 2001, Anti-cancer drugs.

A STRAIGHTFORWARD SYNTHESIS OF O-PROTECTED 3-HYDROXYPROPANAL DERIVATIVES

N. Walchshofer, J. Paris, J. Salvi, 1994 .

A convenient method for the stereoselective preparation of 3-hydroxy-2-substituted propionaldehyde derivatives, C-terminal precursors for the synthesis of trans-alkene dipeptide isosteres

N. Walchshofer, J. Paris, Philippe Roure, 1995, Letters in Peptide Science.

A Straightforward Synthesis of O-Protected 3-Hydroxypropanal Derivatives.

N. Walchshofer, J. Paris, J. Salvi, 1994 .

Peptides 1998, Proceedings of the 25th European Peptide Symposium

C. Rabourdin-Combe, D. Gerlier, D. Tourwé, 1999 .