Michel S - Search Results

1

Synthesis and biological evaluation of dialkylaminoalkylamino benzo[c][1,7] and [1,8]phenanthrolines as antiproliferative agents.

Serbetçi T, Genès C, Depauw S, Prado S, Porée FH, Hildebrand MP, David-Cordonnier MH, Michel S, Tillequin F. Serbetçi T, et al. Among authors: michel s. Eur J Med Chem. 2010 Jun;45(6):2547-58. doi: 10.1016/j.ejmech.2010.02.043. Epub 2010 Feb 25. Eur J Med Chem. 2010. PMID: 20236738

2

Synthesis and cytotoxic activity of benzo[c][1,7] and [1,8]phenanthrolines analogues of nitidine and fagaronine.

Prado S, Michel S, Tillequin F, Koch M, Pfeiffer B, Pierré A, Léonce S, Colson P, Baldeyrou B, Lansiaux A, Bailly C. Prado S, et al. Among authors: michel s. Bioorg Med Chem. 2004 Jul 15;12(14):3943-53. doi: 10.1016/j.bmc.2004.04.038. Bioorg Med Chem. 2004. PMID: 15210161

3

Benzo[b]acronycine derivatives: a novel class of antitumor agents.

Michel S, Gaslonde T, Tillequin F. Michel S, et al. Eur J Med Chem. 2004 Aug;39(8):649-55. doi: 10.1016/j.ejmech.2004.05.001. Eur J Med Chem. 2004. PMID: 15276298 Review.

4

New antitubulin derivatives in the combretastatin A4 series: synthesis and biological evaluation.

Borrel C, Thoret S, Cachet X, Guénard D, Tillequin F, Koch M, Michel S. Borrel C, et al. Among authors: michel s. Bioorg Med Chem. 2005 Jun 1;13(11):3853-64. doi: 10.1016/j.bmc.2005.02.039. Bioorg Med Chem. 2005. PMID: 15863010

5

Synthesis, antitumor activity, and mechanism of action of benzo[a]pyrano[3,2-h]acridin-7-one analogues of acronycine.

Nguyen TM, Sittisombut C, Boutefnouchet S, Lallemand MC, Michel S, Koch M, Tillequin F, Mazinghien R, Lansiaux A, David-Cordonnier MH, Pfeiffer B, Kraus-Berthier L, Léonce S, Pierré A. Nguyen TM, et al. Among authors: michel s. J Med Chem. 2006 Jun 1;49(11):3383-94. doi: 10.1021/jm0602007. J Med Chem. 2006. PMID: 16722658

6

Structure-activity relationships in the acronycine and benzo[b]acronycine series: role of the pyran ring.

Do Q, Thi Mai HD, Gaslonde T, Pfeiffer B, Léonce S, Pierré A, Michel S, Tillequin F, Dufat H. Do Q, et al. Among authors: michel s. Eur J Med Chem. 2008 Dec;43(12):2677-87. doi: 10.1016/j.ejmech.2008.01.033. Epub 2008 Feb 3. Eur J Med Chem. 2008. PMID: 18342404

7

Synthesis, cytotoxic activity, and mechanism of action of furo[2,3-c]acridin-6-one and benzo[b]furo[3,2-h]acridin-6-one analogues of psorospermin and acronycine.

Boutefnouchet S, Gaboriaud-Kolar N, Nguyen TM, Depauw S, David-Cordonnier MH, Pfeiffer B, Léonce S, Pierré A, Tillequin F, Lallemand MC, Michel S. Boutefnouchet S, et al. Among authors: michel s. J Med Chem. 2008 Nov 27;51(22):7287-97. doi: 10.1021/jm8009487. J Med Chem. 2008. PMID: 18947222

8

Synthesis, cytotoxic activity, and DNA binding properties of antitumor cis-1,2-dihydroxy-1,2-dihydrobenzo[b]acronycine cinnamoyl esters.

Do Q, Tian W, Yougnia R, Gaslonde T, Pfeiffer B, Pierré A, Léonce S, Kraus-Berthier L, David-Cordonnier MH, Depauw S, Lansiaux A, Mazinghien R, Koch M, Tillequin F, Michel S, Dufat H. Do Q, et al. Among authors: michel s. Bioorg Med Chem. 2009 Mar 1;17(5):1918-27. doi: 10.1016/j.bmc.2009.01.062. Epub 2009 Jan 31. Bioorg Med Chem. 2009. PMID: 19217791

9

Synthesis and cytotoxic activity of psorospermin and acronycine analogues in the 3-propyloxy-acridin-9(10H)-one and -benzo[b]acridin-125H-one series.

Boutefnouchet S, Minh NT, Putrus R, Pfeiffer B, Léonce S, Pierré A, Michel S, Tillequin F, Lallemand MC. Boutefnouchet S, et al. Among authors: michel s. Eur J Med Chem. 2010 Feb;45(2):581-7. doi: 10.1016/j.ejmech.2009.10.045. Epub 2009 Nov 4. Eur J Med Chem. 2010. PMID: 19926174

10

Structure-activity relationships of indole compounds derived from combretastatin A4: synthesis and biological screening of 5-phenylpyrrolo[3,4-a]carbazole-1,3-diones as potential antivascular agents.

Ty N, Dupeyre G, Chabot GG, Seguin J, Quentin L, Chiaroni A, Tillequin F, Scherman D, Michel S, Cachet X. Ty N, et al. Among authors: michel s. Eur J Med Chem. 2010 Sep;45(9):3726-39. doi: 10.1016/j.ejmech.2010.05.022. Epub 2010 May 15. Eur J Med Chem. 2010. PMID: 20538383

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