F. Ramiandrasoa

发表

Synthesis and Biological Evaluation of Acridine Derivatives as Antimalarial Agents

P. Forterre, B. Pradines, J. Mahy, 2012, ChemMedChem.

Pitumbin, a novel kolavene acylal fromCasearia pitumba pleumer

E. Guittet, C. Moretti, J. Lallemand, 1988 .

In Vitro Potentiation of Antibiotic Activities by a Catecholate Iron Chelator against Chloroquine-Resistant Plasmodium falciparum

C. Rogier, J. Le bras, B. Pradines, 2002, Antimicrobial Agents and Chemotherapy.

Antimalarial acridines: synthesis, in vitro activity against P. falciparum and interaction with hematin.

C. Rogier, B. Pradines, J. Mahy, 2009, Bioorganic & medicinal chemistry.

Evaluation of growth promotion and inhibition from mycobactins and nonmycobacterial siderophores (Desferrioxamine and FR160) in Mycobacterium aurum

A. Andremont, A. Deroussent, G. Kunesch, 1997, Antimicrobial agents and chemotherapy.

Synthesis and in vitro antikinetoplastid activity of polyamine-hydroxybenzotriazole conjugates.

R. Krauth-Siegel, C. Blonski, P. Loiseau, 2017, Bioorganic & medicinal chemistry.

Cellular uptake of a catechol iron chelator and chloroquine into Plasmodium falciparum infected erythrocytes.

C. Rogier, J. Le bras, B. Pradines, 2003, Biochemical pharmacology.

Molluscicidal constituents of Calophyllum from Madagascar: activity of some natural and synthetic neoflavonoids and khellactones.

P. Gayral, N. Kunesch, F. Libot, 1992, Planta medica.

In vitro efficiency of new acridyl derivatives against Plasmodium falciparum.

C. Rogier, B. Pradines, A. Bridoux, 2007, Bioorganic & medicinal chemistry.

Iron chelators as antimalarial agents: in vitro activity of dicatecholate against Plasmodium falciparum.

C. Rogier, J. Le bras, B. Pradines, 2002, The Journal of antimicrobial chemotherapy.

New MnII Complexes with an N/O Coordination Sphere from Tripodal N‐Centered Ligands − Characterization from Solid State to Solution and Reaction with Superoxide in Non‐Aqueous and Aqueous Media

C. Policar, F. Lambert, M. Césario, 2001 .

In vitro activity of iron-binding compounds against Senegalese isolates of Plasmodium falciparum.

C. Rogier, B. Pradines, C. Sokhna, 2006, The Journal of antimicrobial chemotherapy.

In vitro activities of novel catecholate siderophores against Plasmodium falciparum

J. Le bras, B. Pradines, L. Basco, 1996, Antimicrobial agents and chemotherapy.

Siderophore activity of chemically synthesized dihydroxybenzoyl derivatives of spermidines and cystamide

R. Reissbrodt, G. Kunesch, L. Bricard, 1997, Biometals.

Generation of Free Radicals and Enhancement of Hemin-induced Membrane Damage by a Catechol Iron Chelator in Plasmodium falciparum

S. Briolant, C. Rogier, H. Bogreau, 2005 .

A New Highly Stereospecific Synthesis of (E,Z)-2,13-Octadecadienyl Acetate, A Sex Pheromone Component of Some Lepidoptera Species

C. Descoins, F. Ramiandrasoa, 1989 .

A new regioselective synthesis of N1- and N8-monoacylated spermidines

M. Milat, G. Kunesch, F. Ramiandrasoa, 1989 .

Sex pheromones of rice moth,Corcyra cephalonica Stainton

C. Malosse, D. Hall, B. F. Nesbitt, 1987, Journal of Chemical Ecology.

A Convenient Synthesis of the Peach Fruit Moth Carposina Niponensis Walk. and of the Douglas Fir Tussock Moth Orgya Pseudotsugata Mc.D. Sex Pheromones and Analogs

C. Descoins, F. Ramiandrasoa, 1990 .

Kinetics and Thermodynamics of Complex Formation between FeIII and Two Synthetic Chelators of the Dicatecholspermidine Family

G. Kunesch, J. M. Chahine, C. Lion, 2001 .

Design, synthesis and in vitro antikinetoplastid evaluation of N-acylated putrescine, spermidine and spermine derivatives.

C. Blonski, P. Loiseau, S. Pèthe, 2015, Bioorganic & medicinal chemistry letters.