Bailly F - Search Results

1

Relationship between DNA-binding and biological activity of anilinoacridine derivatives containing the nucleic acid-binding unit SPKK.

Bailly F, Bailly C, Helbecque N, Pommery N, Colson P, Houssier C, Hénichart JP. Bailly F, et al. Among authors: bailly c. Anticancer Drug Des. 1992 Feb;7(1):83-100. Anticancer Drug Des. 1992. PMID: 1543529

2

Selective binding to AT sequences in DNA by an acridine-linked peptide containing the SPKK motif.

Bailly F, Bailly C, Waring MJ, Hénichart JP. Bailly F, et al. Among authors: bailly c. Biochem Biophys Res Commun. 1992 Apr 30;184(2):930-7. doi: 10.1016/0006-291x(92)90680-j. Biochem Biophys Res Commun. 1992. PMID: 1315539

3

Interaction of two peptide-acridine conjugates containing the SPKK peptide motif with DNA and chromatin.

Flock S, Bailly F, Bailly C, Waring MJ, Hénichart JP, Colson P, Houssier C. Flock S, et al. Among authors: bailly c, bailly f. J Biomol Struct Dyn. 1994 Feb;11(4):881-900. doi: 10.1080/07391102.1994.10508039. J Biomol Struct Dyn. 1994. PMID: 8204221

4

A tandem repeat of the SPKK peptide motif induces psi-type DNA structures at alternating AT sequences.

Bailly F, Bailly C, Colson P, Houssier C, Hénichart JP. Bailly F, et al. Among authors: bailly c. FEBS Lett. 1993 Jun 14;324(2):181-4. doi: 10.1016/0014-5793(93)81389-h. FEBS Lett. 1993. PMID: 8508919 Free article.

5

Synthesis and biological activities of a series of 4,5-diaryl-3-hydroxy-2(5H)-furanones.

Bailly F, Queffélec C, Mbemba G, Mouscadet JF, Pommery N, Pommery J, Hénichart JP, Cotelle P. Bailly F, et al. Eur J Med Chem. 2008 Jun;43(6):1222-9. doi: 10.1016/j.ejmech.2007.08.005. Epub 2007 Sep 11. Eur J Med Chem. 2008. PMID: 17937972

6

Development of a series of 3-hydroxyquinolin-2(1H)-ones as selective inhibitors of HIV-1 reverse transcriptase associated RNase H activity.

Suchaud V, Bailly F, Lion C, Tramontano E, Esposito F, Corona A, Christ F, Debyser Z, Cotelle P. Suchaud V, et al. Among authors: bailly f. Bioorg Med Chem Lett. 2012 Jun 15;22(12):3988-92. doi: 10.1016/j.bmcl.2012.04.096. Epub 2012 Apr 30. Bioorg Med Chem Lett. 2012. PMID: 22607675

7

Discovery of a cryptic site at the interface 2 of TEAD - Towards a new family of YAP/TAZ-TEAD inhibitors.

Sturbaut M, Bailly F, Coevoet M, Sileo P, Pugniere M, Liberelle M, Magnez R, Thuru X, Chartier-Harlin MC, Melnyk P, Gelin M, Allemand F, Guichou JF, Cotelle P. Sturbaut M, et al. Among authors: bailly f. Eur J Med Chem. 2021 Dec 15;226:113835. doi: 10.1016/j.ejmech.2021.113835. Epub 2021 Sep 6. Eur J Med Chem. 2021. PMID: 34509860

8

Design, synthesis, and anti-integrase activity of catechol-DKA hybrids.

Maurin C, Bailly F, Mbemba G, Mouscadet JF, Cotelle P. Maurin C, et al. Among authors: bailly f. Bioorg Med Chem. 2006 May 1;14(9):2978-84. doi: 10.1016/j.bmc.2005.12.039. Epub 2006 Jan 10. Bioorg Med Chem. 2006. PMID: 16412645

9

The total synthesis of fukiic acid, an HIV-1 integrase inhibitor.

Queffélec C, Bailly F, Mbemba G, Mouscadet JF, Debyser Z, Witvrouw M, Cotelle P. Queffélec C, et al. Among authors: bailly f. Eur J Med Chem. 2008 Oct;43(10):2268-71. doi: 10.1016/j.ejmech.2007.12.013. Epub 2007 Dec 27. Eur J Med Chem. 2008. PMID: 18243421

10

Design, Synthesis and Evaluation of a Series of 1,5-Diaryl-1,2,3-triazole-4-carbohydrazones as Inhibitors of the YAP-TAZ/TEAD Complex.

Gibault F, Sturbaut M, Coevoet M, Pugnière M, Burtscher A, Allemand F, Melnyk P, Hong W, Rubin BP, Pobbati AV, Guichou JF, Cotelle P, Bailly F. Gibault F, et al. Among authors: bailly f. ChemMedChem. 2021 Sep 16;16(18):2823-2844. doi: 10.1002/cmdc.202100153. Epub 2021 Jul 1. ChemMedChem. 2021. PMID: 34032019

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