J. Lancelot

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Novel selective and partial agonists of 5-HT3 receptors. Part 1. Synthesis and biological evaluation of piperazinopyrrolothienopyrazines.

P Delagrange, M. Hamon, B. Guardiola-Lemaitre, 1996, Journal of medicinal chemistry.

Design, synthesis and antiproliferative activity of tripentones: a new series of antitubulin agents.

P. Renard, S. Rault, V. Lisowski, 2001, Bioorganic & medicinal chemistry letters.

Electrochemical behavior of mutagenic nitro and amino derivatives of carbazole

P. Gauduchon, V. André, A. Tallec, 1997 .

Synthesis, Crystal Structure and Interaction With DNA of N,N′-(Butane-1,4-Diyl)Bis(Guanidinium) Tetrachloroplatinate (II)

C. Bailly, G. Morgant, N. Dung, 1998, Metal-based drugs.

Highly Potent and Selective Ligands for a New Class H3 of Histamine Receptor

J. Schwartz, J. Arrang, J. Lecomte, 1988, Investigative radiology.

Effect of cetiedil analogs on acetylcholine and choline fluxes in synaptosomes and vesicles.

M. Robba, M. Diebler, M. Israël, 1989, European journal of pharmacology.

Amoebicidal efficiencies of various diamidines against two strains of Acanthamoeba polyphaga

C. Saturnino, M. Robba, J. Lancelot, 1995, Antimicrobial agents and chemotherapy.

Novel and selective partial agonists of 5-HT3 receptors. 2. Synthesis and biological evaluation of piperazinopyridopyrrolopyrazines, piperazinopyrroloquinoxalines, and piperazinopyridopyrroloquinoxalines.

P Delagrange, M. Hamon, P. Renard, 1997, Journal of medicinal chemistry.

Amide derivatives with H1-antihistaminic effect.

C. Saturnino, G. de Martino, M. Robba, 1998, Pharmaceutica acta Helvetiae.

Synthesis and in vitro evaluation of 4-trichloromethylpyrrolo[1,2-a]quinoxalines as new antiplasmodial agents.

Aurélien Lesnard, S. Rault, N. Azas, 2014, European journal of medicinal chemistry.

Design, synthesis and antiproliferative activity of tripentones: a new series of antitubulin agents.

P. Renard, S. Rault, V. Lisowski, 2001, Bioorganic & medicinal chemistry letters.

Discovery of new thienopyrimidinone derivatives displaying antimalarial properties toward both erythrocytic and hepatic stages of Plasmodium.

Aurélien Lesnard, S. Rault, N. Azas, 2015, European journal of medicinal chemistry.

Biological properties of 5,11-dimethyl-6H-pyrido[3,2-b]carbazoles: a new class of potent antitumour drugs.

L. Poulain, C. Saturnino, P. Gauduchon, 2000, Anti-cancer drug design.

Sequence-selective binding to DNA of bis(amidinophenoxy)alkanes related to propamidine and pentamidine.

M. Waring, C. Bailly, C. Saturnino, 1997, The Biochemical journal.

Tetrachloroplatinates et tetrachloropalladates de N,N'(alkane-dyl)bis(guanidinium) leur preparation et leur application en therapeutique

G. Morgant, M. Robba, J. Lancelot, 1996 .

In vitro cytotoxicity of carbazole derivatives. V. 9-Halogeno-substituted 5,11-dimethyl-6H-pyrido[3,2-b]carbazoles

C. Saturnino, P. Gauduchon, F. Sichel, 1997 .

Synthesis and salidiuretic activity of 2,3-dihydro-8-(1-pyrrolyl)-1,2,4-triazolo[4,3-a]pyridines and 5,6-dihydro-4H-pyrido[2,3-c]pyrrolo[1,2-e]-1,2,5-triazepines.

J. Imbs, M. Barthelmebs, M. Robba, 1991, Chemical & pharmaceutical bulletin.

In vitro cytotoxicity of carbazole derivatives IV. 5,11-Dimethyl-6H-pyrido[3,2-b]carbazoles substituted on the pyridine ring

S. Rault, P. Gauduchon, M. Robba, 1993 .

In vitro effects of Celiptium and MR 14504 on mature rat Leydig cell testosterone production

S. Rault, S. Carreau, M. Robba, 1997, Cell Biology and Toxicology.

Mutagenicity of nitro- and amino-substituted carbazoles in Salmonella typhimurium. III. Methylated derivatives of 9H-carbazole.

C. Mercier, S. Chemtob, P. Gauduchon, 1997, Mutation research.

Comparison of the Effects of Vesamicol and of Cetiedil Analogues on Acetylcholine Release and Vesicular Acetylcholine Transport

M. Robba, M. Israël, M. Diebler, 1991 .

Mutagenicity of nitro- and amino-substituted carbazoles in Salmonella typhimurium. II. Ortho-aminonitro derivatives of 9H-carbazole.

C. Mercier, S. Chemtob, P. Gauduchon, 1995, Mutation research.

Mutagenicity of nitro- and amino-substituted carbazoles in Salmonella typhimurium. I. Monosubstituted derivatives of 9H-carbazole.

S. Rault, C. Saturnino, P. Gauduchon, 1993, Mutation research.

In Vivo Nitric Oxide Synthase Inhibitors Can Be Deprived of This Activity: Unexpected Influence of the Tetrachloroplatinate(II) Counteranion. Crystal Structures of Bis(S-Methyl-Isothiouronium)-N,N′-Bis(3-Guanidinopropyl)Piperazinium and Hexamidinium Tetrachloroplatinates(II) Salts

G. Morgant, P. Prognon, M. Roch-Arveiller, 1998, Metal-based drugs.

In Vivo Inhibition of Nitric Oxide Synthase by Bisisothiouronium and Bisguanidinium Salts

G. Morgant, C. Saturnino, C. Regnault, 1997, European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies.

The Third Histamine Receptor

J. Schwartz, J. Arrang, J. Lecomte, 1989 .

SYNTHESIS, CHARACTERIZATION, AND CRYSTAL STRUCTURE OF THE ISOSTRUCTURAL N,N'-(OCTANE-1,8-DIYL)BIS(GUANIDINIUM) TETRACHLOROPLATINATE (II) AND PALLADATE (II) : ANTIAMEBIC EFFECTS STUDY

G. Morgant, N. Dung, M. Robba, 1997 .