Hunter R - Search Results

1

Structure-activity relationships in 4-aminoquinoline antiplasmodials. The role of the group at the 7-position.

Kaschula CH, Egan TJ, Hunter R, Basilico N, Parapini S, Taramelli D, Pasini E, Monti D. Kaschula CH, et al. Among authors: hunter r. J Med Chem. 2002 Aug 1;45(16):3531-9. doi: 10.1021/jm020858u. J Med Chem. 2002. PMID: 12139464

2

Structure-function relationships in aminoquinolines: effect of amino and chloro groups on quinoline-hematin complex formation, inhibition of beta-hematin formation, and antiplasmodial activity.

Egan TJ, Hunter R, Kaschula CH, Marques HM, Misplon A, Walden J. Egan TJ, et al. Among authors: hunter r. J Med Chem. 2000 Jan 27;43(2):283-91. doi: 10.1021/jm990437l. J Med Chem. 2000. PMID: 10649984

3

Synthesis of 2-deoxy-2-C-alkylglucosides of myo-inositol as possible inhibitors of a N-deacetylase enzyme in the biosynthesis of mycothiol.

Gammon DW, Hunter R, Steenkamp DJ, Mudzunga TT. Gammon DW, et al. Among authors: hunter r. Bioorg Med Chem Lett. 2003 Jun 16;13(12):2045-9. doi: 10.1016/s0960-894x(03)00157-4. Bioorg Med Chem Lett. 2003. PMID: 12781192

4

[d4U]-butyne-[HI-236] as a non-cleavable, bifunctional NRTI/NNRTI HIV-1 reverse-transcriptase inhibitor.

Hunter R, Muhanji CI, Hale I, Bailey CM, Basavapathruni A, Anderson KS. Hunter R, et al. Bioorg Med Chem Lett. 2007 May 1;17(9):2614-7. doi: 10.1016/j.bmcl.2007.01.107. Epub 2007 Feb 4. Bioorg Med Chem Lett. 2007. PMID: 17317163

5

Current developments in the synthesis and biological activity of HIV-1 double-drug inhibitors.

Muhanji CI, Hunter R. Muhanji CI, et al. Among authors: hunter r. Curr Med Chem. 2007;14(11):1207-20. doi: 10.2174/092986707780597952. Curr Med Chem. 2007. PMID: 17504141 Review.

6

Substituted ajoenes as novel anti-cancer agents.

Hunter R, Kaschula CH, Parker IM, Caira MR, Richards P, Travis S, Taute F, Qwebani T. Hunter R, et al. Bioorg Med Chem Lett. 2008 Oct 1;18(19):5277-9. doi: 10.1016/j.bmcl.2008.08.056. Epub 2008 Aug 22. Bioorg Med Chem Lett. 2008. PMID: 18774712

7

C-2-aryl O-substituted HI-236 derivatives as non-nucleoside HIV-1 reverse-transcriptase inhibitors.

Hunter R, Younis Y, Muhanji CI, Curtin TL, Naidoo KJ, Petersen M, Bailey CM, Basavapathruni A, Anderson KS. Hunter R, et al. Bioorg Med Chem. 2008 Dec 15;16(24):10270-80. doi: 10.1016/j.bmc.2008.10.048. Epub 2008 Nov 1. Bioorg Med Chem. 2008. PMID: 18996020 Free PMC article.

8

Garlic-derived anticancer agents: structure and biological activity of ajoene.

Kaschula CH, Hunter R, Parker MI. Kaschula CH, et al. Among authors: hunter r. Biofactors. 2010 Jan-Feb;36(1):78-85. doi: 10.1002/biof.76. Biofactors. 2010. PMID: 20108330 Review.

9

Conjugates of plumbagin and phenyl-2-amino-1-thioglucoside inhibit MshB, a deacetylase involved in the biosynthesis of mycothiol.

Gammon DW, Steenkamp DJ, Mavumengwana V, Marakalala MJ, Mudzunga TT, Hunter R, Munyololo M. Gammon DW, et al. Among authors: hunter r. Bioorg Med Chem. 2010 Apr 1;18(7):2501-14. doi: 10.1016/j.bmc.2010.02.049. Epub 2010 Mar 1. Bioorg Med Chem. 2010. PMID: 20304659

10

[d4U]-spacer-[HI-236] double-drug inhibitors of HIV-1 reverse-transcriptase.

Younis Y, Hunter R, Muhanji CI, Hale I, Singh R, Bailey CM, Sullivan TJ, Anderson KS. Younis Y, et al. Among authors: hunter r. Bioorg Med Chem. 2010 Jul 1;18(13):4661-73. doi: 10.1016/j.bmc.2010.05.025. Epub 2010 May 11. Bioorg Med Chem. 2010. PMID: 20605472 Free PMC article.

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