Carroll FI - Search Results

1

Sex Differences and Drug Dose Influence the Role of the α7 Nicotinic Acetylcholine Receptor in the Mouse Dextran Sodium Sulfate-Induced Colitis Model.

AlSharari SD, Bagdas D, Akbarali HI, Lichtman PA, Raborn ES, Cabral GA, Carroll FI, McGee EA, Damaj MI. AlSharari SD, et al. Among authors: carroll fi. Nicotine Tob Res. 2017 Apr 1;19(4):460-468. doi: 10.1093/ntr/ntw245. Nicotine Tob Res. 2017. PMID: 27639096 Free PMC article.

2

The antinociceptive effects of nicotinic receptors α7-positive allosteric modulators in murine acute and tonic pain models.

Freitas K, Carroll FI, Damaj MI. Freitas K, et al. Among authors: carroll fi. J Pharmacol Exp Ther. 2013 Jan;344(1):264-75. doi: 10.1124/jpet.112.197871. Epub 2012 Oct 31. J Pharmacol Exp Ther. 2013. PMID: 23115222 Free PMC article.

3

In vivo interactions between α7 nicotinic acetylcholine receptor and nuclear peroxisome proliferator-activated receptor-α: Implication for nicotine dependence.

Jackson A, Bagdas D, Muldoon PP, Lichtman AH, Carroll FI, Greenwald M, Miles MF, Damaj MI. Jackson A, et al. Among authors: carroll fi. Neuropharmacology. 2017 May 15;118:38-45. doi: 10.1016/j.neuropharm.2017.03.005. Epub 2017 Mar 7. Neuropharmacology. 2017. PMID: 28279662 Free PMC article.

4

2-Fluoro-3-(4-nitro-phenyl)deschloroepibatidine is a novel potent competitive antagonist of human neuronal alpha4beta2 nAChRs.

Abdrakhmanova GR, Damaj MI, Carroll FI, Martin BR. Abdrakhmanova GR, et al. Among authors: carroll fi. Mol Pharmacol. 2006 Jun;69(6):1945-52. doi: 10.1124/mol.105.021782. Epub 2006 Feb 27. Mol Pharmacol. 2006. PMID: 16505153

5

Synthesis and nicotinic acetylcholine receptor binding properties of bridged and fused ring analogues of epibatidine.

Carroll FI, Robinson TP, Brieaddy LE, Atkinson RN, Mascarella SW, Damaj MI, Martin BR, Navarro HA. Carroll FI, et al. J Med Chem. 2007 Dec 13;50(25):6383-91. doi: 10.1021/jm0704696. Epub 2007 Nov 10. J Med Chem. 2007. PMID: 17994682

6

Synthesis, nicotinic acetylcholine receptor binding, and antinociceptive properties of 3'-(substituted phenyl)epibatidine analogues. Nicotinic partial agonists.

Carroll FI, Ma W, Deng L, Navarro HA, Damaj MI, Martin BR. Carroll FI, et al. J Nat Prod. 2010 Mar 26;73(3):306-12. doi: 10.1021/np9006124. J Nat Prod. 2010. PMID: 20038125 Free PMC article.

7

The antinociceptive effects of nicotinic partial agonists varenicline and sazetidine-A in murine acute and tonic pain models.

AlSharari SD, Carroll FI, McIntosh JM, Damaj MI. AlSharari SD, et al. Among authors: carroll fi. J Pharmacol Exp Ther. 2012 Sep;342(3):742-9. doi: 10.1124/jpet.112.194506. Epub 2012 Jun 7. J Pharmacol Exp Ther. 2012. PMID: 22678099 Free PMC article.

8

Synthesis and nicotinic acetylcholine receptor in vitro and in vivo pharmacological properties of 2'-fluoro-3'-(substituted phenyl)deschloroepibatidine analogues of 2'-fluoro-3'-(4-nitrophenyl)deschloroepibatidine.

Ondachi P, Castro A, Luetje CW, Damaj MI, Mascarella SW, Navarro HA, Carroll FI. Ondachi P, et al. Among authors: carroll fi. J Med Chem. 2012 Jul 26;55(14):6512-22. doi: 10.1021/jm300575y. Epub 2012 Jul 11. J Med Chem. 2012. PMID: 22742586 Free PMC article.

9

Synthesis, nicotinic acetylcholine receptor binding, and antinociceptive properties of 2'-fluoro-3'-(substituted pyridinyl)-7-deschloroepibatidine analogues.

Ondachi PW, Castro AH, Bartkowiak JM, Luetje CW, Damaj MI, Mascarella SW, Navarro HA, Carroll FI. Ondachi PW, et al. Among authors: carroll fi. J Med Chem. 2014 Feb 13;57(3):836-48. doi: 10.1021/jm401602p. Epub 2014 Jan 28. J Med Chem. 2014. PMID: 24428686 Free PMC article.

10

Synthesis, nicotinic acetylcholine receptor binding, in vitro and in vivo pharmacology properties of 3'-(substituted pyridinyl)-deschloroepibatidine analogs.

Ondachi PW, Ye Z, Castro AH, Luetje CW, Damaj MI, Mascarella SW, Navarro HA, Carroll FI. Ondachi PW, et al. Among authors: carroll fi. Bioorg Med Chem. 2015 Sep 1;23(17):5693-701. doi: 10.1016/j.bmc.2015.07.021. Epub 2015 Jul 17. Bioorg Med Chem. 2015. PMID: 26233800 Free PMC article.

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