Grierson DS - Search Results

1

Benzoindoloquinolines interact with DNA tetraplexes and inhibit telomerase.

Alberti P, Schmitt P, Nguyen CH, Rivalle C, Hoarau M, Grierson DS, Mergny JL. Alberti P, et al. Among authors: grierson ds. Bioorg Med Chem Lett. 2002 Apr 8;12(7):1071-4. doi: 10.1016/s0960-894x(02)00080-x. Bioorg Med Chem Lett. 2002. PMID: 11909720

2

Synthesis and evaluation of "AZT-HEPT", "AZT-pyridinone", and "ddC-HEPT" conjugates as inhibitors of HIV reverse transcriptase.

Pontikis R, Dollé V, Guillaumel J, Dechaux E, Note R, Nguyen CH, Legraverend M, Bisagni E, Aubertin AM, Grierson DS, Monneret C. Pontikis R, et al. Among authors: grierson ds. J Med Chem. 2000 May 18;43(10):1927-39. doi: 10.1021/jm991125l. J Med Chem. 2000. PMID: 10821705

3

BENA435, a new cell-permeant photoactivated green fluorescent DNA probe.

Erve A, Saoudi Y, Thirot S, Guetta-Landras C, Florent JC, Nguyen CH, Grierson DS, Popov AV. Erve A, et al. Among authors: grierson ds. Nucleic Acids Res. 2006 Mar 17;34(5):e43. doi: 10.1093/nar/gkl011. Nucleic Acids Res. 2006. PMID: 16547198 Free PMC article.

4

Optimization of triple-helix-directed DNA cleavage by benzoquinoquinoxaline-ethylenediaminetetraacetic acid conjugates.

Zain R, Polverari D, Nguyen CH, Blouquit Y, Bisagni E, Garestier T, Grierson DS, Sun JS. Zain R, et al. Among authors: grierson ds. Chembiochem. 2003 Sep 5;4(9):856-62. doi: 10.1002/cbic.200300621. Chembiochem. 2003. PMID: 12964160

5

Benzoquinoquinoxaline derivatives stabilize and cleave H-DNA and repress transcription downstream of a triplex-forming sequence.

Amiri H, Nekhotiaeva N, Sun JS, Nguyen CH, Grierson DS, Good L, Zain R. Amiri H, et al. Among authors: grierson ds. J Mol Biol. 2005 Aug 26;351(4):776-83. doi: 10.1016/j.jmb.2005.03.044. Epub 2005 Apr 13. J Mol Biol. 2005. PMID: 16045927

6

Triple-helix directed cleavage of double-stranded DNA by benzoquinoquinoxaline-1,10-phenanthroline conjugates.

Zaid A, Sun JS, Nguyen CH, Bisagni E, Garestier T, Grierson DS, Zain R. Zaid A, et al. Among authors: grierson ds. Chembiochem. 2004 Nov 5;5(11):1550-7. doi: 10.1002/cbic.200400074. Chembiochem. 2004. PMID: 15515089

7

Suzuki-type Pd(0) coupling reactions in the synthesis of 2-arylpurines as Cdk inhibitors.

Vandromme L, Piguel S, Lozach O, Meijer L, Legraverend M, Grierson DS. Vandromme L, et al. Among authors: grierson ds. Bioorg Med Chem Lett. 2006 Jun 15;16(12):3144-6. doi: 10.1016/j.bmcl.2006.03.060. Epub 2006 Apr 17. Bioorg Med Chem Lett. 2006. PMID: 16616489

8

3-iodo-4-phenoxypyridinones (IOPY's), a new family of highly potent non-nucleoside inhibitors of HIV-1 reverse transcriptase.

Benjahad A, Guillemont J, Andries K, Nguyen CH, Grierson DS. Benjahad A, et al. Among authors: grierson ds. Bioorg Med Chem Lett. 2003 Dec 15;13(24):4309-12. doi: 10.1016/j.bmcl.2003.09.045. Bioorg Med Chem Lett. 2003. PMID: 14643315

9

Pharmacological inhibition of LIM kinase stabilizes microtubules and inhibits neoplastic growth.

Prudent R, Vassal-Stermann E, Nguyen CH, Pillet C, Martinez A, Prunier C, Barette C, Soleilhac E, Filhol O, Beghin A, Valdameri G, Honoré S, Aci-Sèche S, Grierson D, Antonipillai J, Li R, Di Pietro A, Dumontet C, Braguer D, Florent JC, Knapp S, Bernard O, Lafanechère L. Prudent R, et al. Cancer Res. 2012 Sep 1;72(17):4429-39. doi: 10.1158/0008-5472.CAN-11-3342. Epub 2012 Jul 3. Cancer Res. 2012. PMID: 22761334 Free article.

10

The purines: potent and versatile small molecule inhibitors and modulators of key biological targets.

Legraverend M, Grierson DS. Legraverend M, et al. Among authors: grierson ds. Bioorg Med Chem. 2006 Jun 15;14(12):3987-4006. doi: 10.1016/j.bmc.2005.12.060. Epub 2006 Feb 24. Bioorg Med Chem. 2006. PMID: 16503144 Review.

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