Storer R - Search Results

1

Discovery of the Aryl-phospho-indole IDX899, a Highly Potent Anti-HIV Non-nucleoside Reverse Transcriptase Inhibitor.

Dousson C, Alexandre FR, Amador A, Bonaric S, Bot S, Caillet C, Convard T, da Costa D, Lioure MP, Roland A, Rosinovsky E, Maldonado S, Parsy C, Trochet C, Storer R, Stewart A, Wang J, Mayes BA, Musiu C, Poddesu B, Vargiu L, Liuzzi M, Moussa A, Jakubik J, Hubbard L, Seifer M, Standring D. Dousson C, et al. Among authors: storer r. J Med Chem. 2016 Mar 10;59(5):1891-8. doi: 10.1021/acs.jmedchem.5b01430. Epub 2016 Feb 3. J Med Chem. 2016. PMID: 26804933

2

Synthesis and biological evaluation of aryl-phospho-indole as novel HIV-1 non-nucleoside reverse transcriptase inhibitors.

Alexandre FR, Amador A, Bot S, Caillet C, Convard T, Jakubik J, Musiu C, Poddesu B, Vargiu L, Liuzzi M, Roland A, Seifer M, Standring D, Storer R, Dousson CB. Alexandre FR, et al. Among authors: storer r. J Med Chem. 2011 Jan 13;54(1):392-5. doi: 10.1021/jm101142k. Epub 2010 Dec 13. J Med Chem. 2011. PMID: 21142105

3

Synthesis and pharmacokinetics of valopicitabine (NM283), an efficient prodrug of the potent anti-HCV agent 2'-C-methylcytidine.

Pierra C, Amador A, Benzaria S, Cretton-Scott E, D'Amours M, Mao J, Mathieu S, Moussa A, Bridges EG, Standring DN, Sommadossi JP, Storer R, Gosselin G. Pierra C, et al. Among authors: storer r. J Med Chem. 2006 Nov 2;49(22):6614-20. doi: 10.1021/jm0603623. J Med Chem. 2006. PMID: 17064080

4

Synthesis and antiviral evaluation of thieno[3,4-d]pyrimidine C-nucleoside analogues of 2',3'-dideoxy- and 2',3'-dideoxy-2',3'-didehydro-adenosine and -inosine.

Hamann M, Pierra C, Sommadossi JP, Musiu C, Vargiu L, Liuzzi M, Storer R, Gosselin G. Hamann M, et al. Among authors: storer r. Bioorg Med Chem. 2009 Mar 15;17(6):2321-6. doi: 10.1016/j.bmc.2009.02.011. Epub 2009 Feb 14. Bioorg Med Chem. 2009. PMID: 19254848

5

2'-C-Methyl branched pyrimidine ribonucleoside analogues: potent inhibitors of RNA virus replication.

Benzaria S, Bardiot D, Bouisset T, Counor C, Rabeson C, Pierra C, Storer R, Loi AG, Cadeddu A, Mura M, Musiu C, Liuzzi M, Loddo R, Bergelson S, Bichko V, Bridges E, Cretton-Scott E, Mao J, Sommadossi JP, Seifer M, Standring D, Tausek M, Gosselin G, La Colla P. Benzaria S, et al. Among authors: storer r. Antivir Chem Chemother. 2007;18(4):225-42. doi: 10.1177/095632020701800406. Antivir Chem Chemother. 2007. PMID: 17907380 Free article.

6

Synthesis and antiviral evaluation of a seven-membered sugar ring nucleoside analog, 9-(5-deoxy-beta-D-allo-septanosyl)-adenine.

Sizun G, Griffon JF, Griffe L, Dukhan D, Storer R, Sommadossi JP, Loi AG, Musiu C, Poddesu B, Cadeddu A, Fanti M, Boscu N, Bassetti F, Liuzzi M, Gosselin G. Sizun G, et al. Among authors: storer r. Nucleic Acids Symp Ser (Oxf). 2008;(52):611-2. doi: 10.1093/nass/nrn309. Nucleic Acids Symp Ser (Oxf). 2008. PMID: 18776528

7

Nm 283, an efficient prodrug of the potent anti-HCV agent 2'-C-methylcytidine.

Pierra C, Benzaria S, Amador A, Moussa A, Mathieu S, Storer R, Gosselin G. Pierra C, et al. Among authors: storer r. Nucleosides Nucleotides Nucleic Acids. 2005;24(5-7):767-70. doi: 10.1081/ncn-200060112. Nucleosides Nucleotides Nucleic Acids. 2005. PMID: 16248033

8

Synthesis and antiviral evaluation of 7-fluoro-7-deaza-2-aminopurine nucleoside derivatives.

Leroy F, Chaves D, Dukhan D, Storer R, Sommadossi JP, Loi AG, Cadeddu A, Fanti M, Boscu N, Bassetti F, Liuzzi M, Gosselin G. Leroy F, et al. Among authors: storer r. Nucleic Acids Symp Ser (Oxf). 2008;(52):595-6. doi: 10.1093/nass/nrn301. Nucleic Acids Symp Ser (Oxf). 2008. PMID: 18776520

9

Synthesis and antiviral evaluation of 4-fluoropyrazole-3-carboxamide nucleoside derivatives.

Leroy F, Chaves D, Dukhan D, Storer R, Sommadossi JP, Loi AG, Cadeddu A, Fanti M, Boscu N, Bassetti F, Liuzzi M, Gosselin G. Leroy F, et al. Among authors: storer r. Nucleic Acids Symp Ser (Oxf). 2008;(52):617-8. doi: 10.1093/nass/nrn312. Nucleic Acids Symp Ser (Oxf). 2008. PMID: 18776531

10

Discovery of Clinical Candidate 4-[2-(5-Amino-1H-pyrazol-4-yl)-4-chlorophenoxy]-5-chloro-2-fluoro-N-1,3-thiazol-4-ylbenzenesulfonamide (PF-05089771): Design and Optimization of Diaryl Ether Aryl Sulfonamides as Selective Inhibitors of Na_V1.7.

Swain NA, Batchelor D, Beaudoin S, Bechle BM, Bradley PA, Brown AD, Brown B, Butcher KJ, Butt RP, Chapman ML, Denton S, Ellis D, Galan SRG, Gaulier SM, Greener BS, de Groot MJ, Glossop MS, Gurrell IK, Hannam J, Johnson MS, Lin Z, Markworth CJ, Marron BE, Millan DS, Nakagawa S, Pike A, Printzenhoff D, Rawson DJ, Ransley SJ, Reister SM, Sasaki K, Storer RI, Stupple PA, West CW. Swain NA, et al. Among authors: storer ri. J Med Chem. 2017 Aug 24;60(16):7029-7042. doi: 10.1021/acs.jmedchem.7b00598. Epub 2017 Aug 10. J Med Chem. 2017. PMID: 28682065

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