Campbell EA - Search Results

1

In vivo pharmacology of SDZ 249-665, a novel, non-pungent capsaicin analogue.

Urban L, Campbell EA, Panesar M, Patel S, Chaudhry N, Kane S, Buchheit KH, Sandells B, James IF. Urban L, et al. Among authors: campbell ea. Pain. 2000 Dec 15;89(1):65-74. doi: 10.1016/S0304-3959(00)00349-3. Pain. 2000. PMID: 11113294

2

Oral anti-hyperalgesic and anti-inflammatory activity of NK(1) receptor antagonists in models of inflammatory hyperalgesia of the guinea-pig.

Campbell EA, Gentry C, Patel S, Kidd B, Cruwys S, Fox AJ, Urban L. Campbell EA, et al. Pain. 2000 Sep;87(3):253-263. doi: 10.1016/S0304-3959(00)00288-8. Pain. 2000. PMID: 10963905

3

Comparative, general pharmacology of SDZ NKT 343, a novel, selective NK1 receptor antagonist.

Walpole CS, Brown MC, James IF, Campbell EA, McIntyre P, Docherty R, Ko S, Hedley L, Ewan S, Buchheit KH, Urban LA. Walpole CS, et al. Among authors: campbell ea. Br J Pharmacol. 1998 May;124(1):83-92. doi: 10.1038/sj.bjp.0701806. Br J Pharmacol. 1998. PMID: 9630347 Free PMC article.

4

2-Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N-benzyl-N - methylamide (SDZ NKT 343), a potent human NK1 tachykinin receptor antagonist with good oral analgesic activity in chronic pain models.

Walpole C, Ko SY, Brown M, Beattie D, Campbell E, Dickenson F, Ewan S, Hughes GA, Lemaire M, Lerpiniere J, Patel S, Urban L. Walpole C, et al. J Med Chem. 1998 Aug 13;41(17):3159-73. doi: 10.1021/jm970499g. J Med Chem. 1998. PMID: 9703462

5

Analogues of capsaicin with agonist activity as novel analgesic agents; structure-activity studies. 1. The aromatic "A-region".

Walpole CS, Wrigglesworth R, Bevan S, Campbell EA, Dray A, James IF, Perkins MN, Reid DJ, Winter J. Walpole CS, et al. Among authors: campbell ea. J Med Chem. 1993 Aug 6;36(16):2362-72. doi: 10.1021/jm00068a014. J Med Chem. 1993. PMID: 8360881

6

Analogues of capsaicin with agonist activity as novel analgesic agents; structure-activity studies. 2. The amide bond "B-region".

Walpole CS, Wrigglesworth R, Bevan S, Campbell EA, Dray A, James IF, Masdin KJ, Perkins MN, Winter J. Walpole CS, et al. Among authors: campbell ea. J Med Chem. 1993 Aug 6;36(16):2373-80. doi: 10.1021/jm00068a015. J Med Chem. 1993. PMID: 8360882

7

Analogues of capsaicin with agonist activity as novel analgesic agents; structure-activity studies. 3. The hydrophobic side-chain "C-region".

Walpole CS, Wrigglesworth R, Bevan S, Campbell EA, Dray A, James IF, Masdin KJ, Perkins MN, Winter J. Walpole CS, et al. Among authors: campbell ea. J Med Chem. 1993 Aug 6;36(16):2381-9. doi: 10.1021/jm00068a016. J Med Chem. 1993. PMID: 8360883

8

Selective neurokinin-1 receptor antagonists are anti-hyperalgesic in a model of neuropathic pain in the guinea-pig.

Campbell EA, Gentry CT, Patel S, Panesar MS, Walpole CS, Urban L. Campbell EA, et al. Neuroscience. 1998 Dec;87(3):527-32. doi: 10.1016/s0306-4522(98)00318-2. Neuroscience. 1998. PMID: 9758219

9

Analogues of capsaicin with agonist activity as novel analgesic agents: structure-activity studies. 4. Potent, orally active analgesics.

Wrigglesworth R, Walpole CS, Bevan S, Campbell EA, Dray A, Hughes GA, James I, Masdin KJ, Winter J. Wrigglesworth R, et al. Among authors: campbell ea. J Med Chem. 1996 Dec 6;39(25):4942-51. doi: 10.1021/jm960512h. J Med Chem. 1996. PMID: 8960554

10

Antinociceptive activity of the bradykinin B1 and B2 receptor antagonists, des-Arg9, [Leu8]-BK and HOE 140, in two models of persistent hyperalgesia in the rat.

Perkins MN, Campbell E, Dray A. Perkins MN, et al. Pain. 1993 May;53(2):191-197. doi: 10.1016/0304-3959(93)90080-9. Pain. 1993. PMID: 8393171

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