Brown J - Search Results

1

GW627368X ((N-{2-[4-(4,9-diethoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetyl} benzene sulphonamide): a novel, potent and selective prostanoid EP4 receptor antagonist.

Wilson RJ, Giblin GM, Roomans S, Rhodes SA, Cartwright KA, Shield VJ, Brown J, Wise A, Chowdhury J, Pritchard S, Coote J, Noel LS, Kenakin T, Burns-Kurtis CL, Morrison V, Gray DW, Giles H. Wilson RJ, et al. Among authors: brown j. Br J Pharmacol. 2006 Jun;148(3):326-39. doi: 10.1038/sj.bjp.0706726. Br J Pharmacol. 2006. PMID: 16604093 Free PMC article.

2

Pharmacology of GPR55 in yeast and identification of GSK494581A as a mixed-activity glycine transporter subtype 1 inhibitor and GPR55 agonist.

Brown AJ, Daniels DA, Kassim M, Brown S, Haslam CP, Terrell VR, Brown J, Nichols PL, Staton PC, Wise A, Dowell SJ. Brown AJ, et al. Among authors: brown s, brown j. J Pharmacol Exp Ther. 2011 Apr;337(1):236-46. doi: 10.1124/jpet.110.172650. Epub 2011 Jan 13. J Pharmacol Exp Ther. 2011. PMID: 21233197

3

Little or no ability of obestatin to interact with ghrelin or modify motility in the rat gastrointestinal tract.

Bassil AK, Häglund Y, Brown J, Rudholm T, Hellström PM, Näslund E, Lee K, Sanger GJ. Bassil AK, et al. Among authors: brown j. Br J Pharmacol. 2007 Jan;150(1):58-64. doi: 10.1038/sj.bjp.0706969. Epub 2006 Nov 27. Br J Pharmacol. 2007. PMID: 17128285 Free PMC article.

4

Use of a dual firefly and Renilla luciferase reporter gene assay to simultaneously determine drug selectivity at human corticotrophin releasing hormone 1 and 2 receptors.

Parsons SJ, Rhodes SA, Connor HE, Rees S, Brown J, Giles H. Parsons SJ, et al. Among authors: brown j. Anal Biochem. 2000 Jun 1;281(2):187-92. doi: 10.1006/abio.2000.4570. Anal Biochem. 2000. PMID: 10870834

5

Modulation of peristalsis by NK3 receptor antagonism in guinea-pig isolated ileum is revealed as intraluminal pressure is raised.

Sanger GJ, Tuladhar BR, Brown J, Aziz E, Sivakumar D, Furness JB. Sanger GJ, et al. Among authors: brown j. Auton Autacoid Pharmacol. 2007 Apr;27(2):105-11. doi: 10.1111/j.1474-8673.2007.00396.x. Auton Autacoid Pharmacol. 2007. PMID: 17391280

6

The amino terminus of receptor activity modifying proteins is a critical determinant of glycosylation state and ligand binding of calcitonin receptor-like receptor.

Fraser NJ, Wise A, Brown J, McLatchie LM, Main MJ, Foord SM. Fraser NJ, et al. Among authors: brown j. Mol Pharmacol. 1999 Jun;55(6):1054-9. doi: 10.1124/mol.55.6.1054. Mol Pharmacol. 1999. PMID: 10347248

7

Inhibition of colonic motility and defecation by RS-127445 suggests an involvement of the 5-HT2B receptor in rodent large bowel physiology.

Bassil AK, Taylor CM, Bolton VJ, Gray KM, Brown JD, Cutler L, Summerfield SG, Bruton G, Winchester WJ, Lee K, Sanger GJ. Bassil AK, et al. Among authors: brown jd. Br J Pharmacol. 2009 Sep;158(1):252-8. doi: 10.1111/j.1476-5381.2009.00155.x. Epub 2009 Apr 9. Br J Pharmacol. 2009. PMID: 19371340 Free PMC article.

8

The N-terminus of RAMPs is a critical determinant of the glycosylation state and ligand binding of calcitonin receptor-like receptor.

Foord SM, Wise A, Brown J, Main MJ, Fraser NJ. Foord SM, et al. Among authors: brown j. Biochem Soc Trans. 1999 Aug;27(4):535-9. doi: 10.1042/bst0270535. Biochem Soc Trans. 1999. PMID: 10917636 Review. No abstract available.

9

GR196429: a nonindolic agonist at high-affinity melatonin receptors.

Beresford IJ, Browning C, Starkey SJ, Brown J, Foord SM, Coughlan J, North PC, Dubocovich ML, Hagan RM. Beresford IJ, et al. Among authors: brown j. J Pharmacol Exp Ther. 1998 Jun;285(3):1239-45. J Pharmacol Exp Ther. 1998. PMID: 9618428

10

Pharmacological activity of VUF 9153, an isothiourea histamine H3 receptor antagonist.

Barnes JC, Brown JD, Clarke NP, Clapham J, Evans DJ, O'Shaughnessy CT. Barnes JC, et al. Among authors: brown jd. Eur J Pharmacol. 1993 Nov 30;250(1):147-52. doi: 10.1016/0014-2999(93)90632-r. Eur J Pharmacol. 1993. PMID: 8119312

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