Barbe J - Search Results

1

Effects of a series of dihydroanthracene derivatives on drug efflux in multidrug resistant cancer cells.

Alibert S, Santelli-Rouvier C, Castaing M, Berthelot M, Spengler G, Molnar J, Barbe J. Alibert S, et al. Among authors: barbe j. Eur J Med Chem. 2003 Mar;38(3):253-63. doi: 10.1016/s0223-5234(03)00018-7. Eur J Med Chem. 2003. PMID: 12667692

2

Synthesis and effects on chloroquine susceptibility in Plasmodium falciparum of a series of new dihydroanthracene derivatives.

Alibert S, Santelli-Rouvier C, Pradines B, Houdoin C, Parzy D, Karolak-Wojciechowska J, Barbe J. Alibert S, et al. Among authors: barbe j. J Med Chem. 2002 Jul 18;45(15):3195-209. doi: 10.1021/jm011046l. J Med Chem. 2002. PMID: 12109904

3

Synthesis of aza mono, bi and tricyclic compounds. Evaluation of their anti MDR activity.

Gallo S, Atifi S, Mahamoud A, Santelli-Rouvier C, Wolfárt K, Molnar J, Barbe J. Gallo S, et al. Among authors: barbe j. Eur J Med Chem. 2003 Jan;38(1):19-26. doi: 10.1016/s0223-5234(02)01422-8. Eur J Med Chem. 2003. PMID: 12593913

4

Arylsulfonyl acridinyl derivatives acting on Plasmodium falciparum.

Santelli-Rouvier C, Pradines B, Berthelot M, Parzy D, Barbe J. Santelli-Rouvier C, et al. Among authors: barbe j. Eur J Med Chem. 2004 Sep;39(9):735-44. doi: 10.1016/j.ejmech.2004.05.007. Eur J Med Chem. 2004. PMID: 15337286

5

Synthesis of 9-acridinyl sulfur derivatives: sulfides, sulfoxides and sulfones. Comparison of their activity on tumour cells.

Santelli-Rouvier C, Barret JM, Farrell CM, Sharples D, Hill BT, Barbe J. Santelli-Rouvier C, et al. Among authors: barbe j. Eur J Med Chem. 2004 Dec;39(12):1029-38. doi: 10.1016/j.ejmech.2004.06.015. Eur J Med Chem. 2004. PMID: 15571864

6

In vitro increase in chloroquine accumulation induced by dihydroethano- and ethenoanthracene derivatives in Plasmodium falciparum-parasitized erythrocytes.

Pradines B, Alibert S, Houdoin C, Santelli-Rouvier C, Mosnier J, Fusai T, Rogier C, Barbe J, Parzy D. Pradines B, et al. Among authors: barbe j. Antimicrob Agents Chemother. 2002 Jul;46(7):2061-8. doi: 10.1128/AAC.46.7.2061-2068.2002. Antimicrob Agents Chemother. 2002. PMID: 12069956 Free PMC article.

7

Membrane permeation by multidrug-resistance-modulators and non-modulators: effects of hydrophobicity and electric charge.

Castaing M, Brouant P, Loiseau A, Santelli-Rouvier C, Santelli M, Alibert-Franco S, Mahamoud A, Barbe J. Castaing M, et al. Among authors: barbe j. J Pharm Pharmacol. 2000 Mar;52(3):289-96. doi: 10.1211/0022357001773977. J Pharm Pharmacol. 2000. PMID: 10757416

8

Inhibition of efflux of quinolines as new therapeutic strategy in malaria.

Henry M, Alibert S, Rogier C, Barbe J, Pradines B. Henry M, et al. Among authors: barbe j. Curr Top Med Chem. 2008;8(7):563-78. doi: 10.2174/156802608783955593. Curr Top Med Chem. 2008. PMID: 18473883 Review.

9

Inhibition of Trypanosoma cruzi trypanothione reductase by acridines: kinetic studies and structure-activity relationships.

Bonse S, Santelli-Rouvier C, Barbe J, Krauth-Siegel RL. Bonse S, et al. Among authors: barbe j. J Med Chem. 1999 Dec 30;42(26):5448-54. doi: 10.1021/jm990386s. J Med Chem. 1999. PMID: 10639286

10

The interaction between resistance modifiers such as pyrido[3,2-g]quinoline, aza-oxafluorene and pregnane derivatives with DNA, plasmid DNA and tRNA.

Sharples D, Spengler G, Molnár J, Antal Z, Molnár A, Kiss JT, Szabó JA, Hilgeroth A, Gallo S, Mahamoud A, Barbe J. Sharples D, et al. Among authors: barbe j. Eur J Med Chem. 2005 Feb;40(2):195-202. doi: 10.1016/j.ejmech.2004.10.011. Eur J Med Chem. 2005. PMID: 15694654

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