Clark RD - Search Results

1

RS 23597-190: a potent and selective 5-HT4 receptor antagonist.

Eglen RM, Bley K, Bonhaus DW, Clark RD, Hegde SS, Johnson LG, Leung E, Wong EH. Eglen RM, et al. Among authors: clark rd. Br J Pharmacol. 1993 Sep;110(1):119-26. doi: 10.1111/j.1476-5381.1993.tb13780.x. Br J Pharmacol. 1993. PMID: 8220871 Free PMC article.

2

The interaction of RS 25259-197, a potent and selective antagonist, with 5-HT3 receptors, in vitro.

Wong EH, Clark R, Leung E, Loury D, Bonhaus DW, Jakeman L, Parnes H, Whiting RL, Eglen RM. Wong EH, et al. Br J Pharmacol. 1995 Feb;114(4):851-9. doi: 10.1111/j.1476-5381.1995.tb13282.x. Br J Pharmacol. 1995. PMID: 7773546 Free PMC article.

3

Pharmacological characterization of RS 25259-197, a novel and selective 5-HT3 receptor antagonist, in vivo.

Eglen RM, Lee CH, Smith WL, Johnson LG, Clark R, Whiting RL, Hegde SS. Eglen RM, et al. Br J Pharmacol. 1995 Feb;114(4):860-6. doi: 10.1111/j.1476-5381.1995.tb13283.x. Br J Pharmacol. 1995. PMID: 7773547 Free PMC article.

4

Investigation of the prostacyclin (IP) receptor antagonist RO1138452 on isolated blood vessel and platelet preparations.

Jones RL, Wise H, Clark R, Whiting RL, Bley KR. Jones RL, et al. Br J Pharmacol. 2006 Sep;149(1):110-20. doi: 10.1038/sj.bjp.0706841. Epub 2006 Jul 31. Br J Pharmacol. 2006. PMID: 16880763 Free PMC article.

5

(R) and (S) RS 56532: mixed 5-HT3 and 5-HT4 receptor ligands with opposing enantiomeric selectivity.

Eglen RM, Bonhaus DW, Clark RD, Johnson LG, Lee CH, Leung E, Smith WL, Wong EH, Whiting RL. Eglen RM, et al. Among authors: clark rd. Neuropharmacology. 1994 Mar-Apr;33(3-4):515-26. doi: 10.1016/0028-3908(94)90083-3. Neuropharmacology. 1994. PMID: 7984291

6

Pharmacological characterization of two novel and potent 5-HT4 receptor agonists, RS 67333 and RS 67506, in vitro and in vivo.

Eglen RM, Bonhaus DW, Johnson LG, Leung E, Clark RD. Eglen RM, et al. Among authors: clark rd. Br J Pharmacol. 1995 Aug;115(8):1387-92. doi: 10.1111/j.1476-5381.1995.tb16628.x. Br J Pharmacol. 1995. PMID: 8564196 Free PMC article.

7

Comparison of 5-HT4 receptors in guinea-pig colon and rat oesophagus: effects of novel agonists and antagonists.

Leung E, Pulido-Rios MT, Bonhaus DW, Pekins LA, Zeitung KD, Hsu SA, Clark RD, Wong EH, Eglen RM. Leung E, et al. Among authors: clark rd. Naunyn Schmiedebergs Arch Pharmacol. 1996 Jul;354(2):145-56. doi: 10.1007/BF00178714. Naunyn Schmiedebergs Arch Pharmacol. 1996. PMID: 8857591

8

[3H]RS 57639, a high affinity, selective 5-HT4 receptor partial agonist, specifically labels guinea-pig striatal and rat cloned (5-HT4S and 5-HT4L) receptors.

Bonhaus DW, Berger J, Adham N, Branchek TA, Hsu SA, Loury DN, Leung E, Wong EH, Clark RD, Eglen RM. Bonhaus DW, et al. Among authors: clark rd. Neuropharmacology. 1997 Apr-May;36(4-5):671-9. doi: 10.1016/s0028-3908(97)00039-7. Neuropharmacology. 1997. PMID: 9225293

9

RS 39604: a potent, selective and orally active 5-HT4 receptor antagonist.

Hegde SS, Bonhaus DW, Johnson LG, Leung E, Clark RD, Eglen RM. Hegde SS, et al. Among authors: clark rd. Br J Pharmacol. 1995 Jul;115(6):1087-95. doi: 10.1111/j.1476-5381.1995.tb15922.x. Br J Pharmacol. 1995. PMID: 7582507 Free PMC article.

10

2-(Quinuclidin-3-yl)pyrido[4,3-b]indol-1-ones and isoquinolin-1-ones. Potent conformationally restricted 5-HT3 receptor antagonists.

Clark RD, Miller AB, Berger J, Repke DB, Weinhardt KK, Kowalczyk BA, Eglen RM, Bonhaus DW, Lee CH, Michel AD, et al. Clark RD, et al. J Med Chem. 1993 Sep 3;36(18):2645-57. doi: 10.1021/jm00070a008. J Med Chem. 1993. PMID: 8410977

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