Hicks RP - Search Results

1

Structure-activity relationship study of antimalarial indolo [2,1-b]quinazoline-6,12-diones (tryptanthrins). Three dimensional pharmacophore modeling and identification of new antimalarial candidates.

Bhattacharjee AK, Hartell MG, Nichols DA, Hicks RP, Stanton B, van Hamont JE, Milhous WK. Bhattacharjee AK, et al. Among authors: hicks rp. Eur J Med Chem. 2004 Jan;39(1):59-67. doi: 10.1016/j.ejmech.2003.10.004. Eur J Med Chem. 2004. PMID: 14987834

2

Nuclear magnetic resonance and molecular modeling analysis of the interaction of the antimalarial drugs artelinic acid and artesunic acid with beta-cyclodextrin.

Hartell MG, Hicks R, Bhattacharjee AK, Koser BW, Carvalho K, Van Hamont JE. Hartell MG, et al. J Pharm Sci. 2004 Aug;93(8):2076-89. doi: 10.1002/jps.20106. J Pharm Sci. 2004. PMID: 15236456

3

The medicinal chemistry of botulinum, ricin and anthrax toxins.

Hicks RP, Hartell MG, Nichols DA, Bhattacharjee AK, van Hamont JE, Skillman DR. Hicks RP, et al. Curr Med Chem. 2005;12(6):667-90. doi: 10.2174/0929867053202223. Curr Med Chem. 2005. PMID: 15790305 Review.

4

The anthrax protective antigen (PA63) bound conformation of a peptide inhibitor of the binding of lethal factor to PA63: as determined by trNOESY NMR and molecular modeling.

Hicks RP, Bhattacharjee AK, Koser BW, Traficante DD. Hicks RP, et al. J Med Chem. 2004 Oct 21;47(22):5347-55. doi: 10.1021/jm040139a. J Med Chem. 2004. PMID: 15481973

5

Comparison of the conformation and electrostatic surface properties of magainin peptides bound to sodium dodecyl sulfate and dodecylphosphocholine micelles.

Hicks RP, Mones E, Kim H, Koser BW, Nichols DA, Bhattacharjee AK. Hicks RP, et al. Biopolymers. 2003 Apr;68(4):459-70. doi: 10.1002/bip.10325. Biopolymers. 2003. PMID: 12666172

6

Application of 3D-QSAR for identification of descriptors defining bioactivity of antimicrobial peptides.

Bhonsle JB, Venugopal D, Huddler DP, Magill AJ, Hicks RP. Bhonsle JB, et al. Among authors: hicks rp. J Med Chem. 2007 Dec 27;50(26):6545-53. doi: 10.1021/jm070884y. Epub 2007 Dec 7. J Med Chem. 2007. PMID: 18062663

7

De novo design of selective antibiotic peptides by incorporation of unnatural amino acids.

Hicks RP, Bhonsle JB, Venugopal D, Koser BW, Magill AJ. Hicks RP, et al. J Med Chem. 2007 Jun 28;50(13):3026-36. doi: 10.1021/jm061489v. Epub 2007 Jun 5. J Med Chem. 2007. PMID: 17547385

8

Novel antimicrobial peptides that exhibit activity against select agents and other drug resistant bacteria.

Venugopal D, Klapper D, Srouji AH, Bhonsle JB, Borschel R, Mueller A, Russell AL, Williams BC, Hicks RP. Venugopal D, et al. Among authors: hicks rp. Bioorg Med Chem. 2010 Jul 15;18(14):5137-47. doi: 10.1016/j.bmc.2010.05.065. Epub 2010 May 27. Bioorg Med Chem. 2010. PMID: 20558071

9

Spectral and biological evaluation of a synthetic antimicrobial peptide derived from 1-aminocyclohexane carboxylic acid.

Abercrombie JJ, Leung KP, Chai H, Hicks RP. Abercrombie JJ, et al. Among authors: hicks rp. Bioorg Med Chem. 2015 Mar 15;23(6):1341-7. doi: 10.1016/j.bmc.2015.01.027. Epub 2015 Jan 22. Bioorg Med Chem. 2015. PMID: 25684423

10

The effect of the placement and total charge of the basic amino acid clusters on antibacterial organism selectivity and potency.

Russell AL, Spuches AM, Williams BC, Venugopal D, Klapper D, Srouji AH, Hicks RP. Russell AL, et al. Among authors: hicks rp. Bioorg Med Chem. 2011 Dec 1;19(23):7008-22. doi: 10.1016/j.bmc.2011.10.033. Epub 2011 Oct 18. Bioorg Med Chem. 2011. PMID: 22047803

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