Ohnmacht CJ - Search Results

1

ZENECA ZD6169: a novel KATP channel opener with in vivo selectivity for urinary bladder.

Howe BB, Halterman TJ, Yochim CL, Do ML, Pettinger SJ, Stow RB, Ohnmacht CJ, Russell K, Empfield JR, Trainor DA, et al. Howe BB, et al. Among authors: ohnmacht cj. J Pharmacol Exp Ther. 1995 Aug;274(2):884-90. J Pharmacol Exp Ther. 1995. PMID: 7636752

2

Calcium dependent K-channels in guinea pig and human urinary bladder.

Trivedi S, Potter-Lee L, Li JH, Yasay GD, Russell K, Ohnmacht CJ, Empfield JR, Trainor DA, Kau ST. Trivedi S, et al. Among authors: ohnmacht cj. Biochem Biophys Res Commun. 1995 Aug 15;213(2):404-9. doi: 10.1006/bbrc.1995.2146. Biochem Biophys Res Commun. 1995. PMID: 7544120

3

K-channel opening activity of ZD6169 and its analogs: effect on 86Rb efflux and 3H-P1075 binding in bladder smooth muscle.

Trivedi S, Stetz SL, Potter-Lee L, McConville M, Li JH, Empfield J, Ohnmacht CJ, Russell K, Brown FJ, Trainor DA, et al. Trivedi S, et al. Among authors: ohnmacht cj. Pharmacology. 1995 Jun;50(6):388-97. doi: 10.1159/000139308. Pharmacology. 1995. PMID: 7568338

4

Zeneca ZD6169 and its analogs from a novel series of anilide tertiary carbinols: in vitro KATP channel opening activity in bladder detrusor.

Li JH, Yasay GD, Zografos P, Kau ST, Ohnmacht CJ, Russell K, Empfield JR, Brown FJ, Trainor DA, Bonev AD, et al. Li JH, et al. Among authors: ohnmacht cj. Pharmacology. 1995 Jun;51(1):33-42. doi: 10.1159/000139314. Pharmacology. 1995. PMID: 7568342

5

N-aryl-3,3,3-trifluoro-2-hydroxy-2-methylpropanamides: KATP potassium channel openers. Modifications on the western region.

Ohnmacht CJ, Russell K, Empfield JR, Frank CA, Gibson KH, Mayhugh DR, McLaren FM, Shapiro HS, Brown FJ, Trainor DA, Ceccarelli C, Lin MM, Masek BB, Forst JM, Harris RJ, Hulsizer JM, Lewis JJ, Silverman SM, Smith RW, Warwick PJ, Kau ST, Chun AL, Grant TL, Howe BB, Neilson KL, et al. Ohnmacht CJ, et al. J Med Chem. 1996 Nov 8;39(23):4592-601. doi: 10.1021/jm960365n. J Med Chem. 1996. PMID: 8917648

6

K-channel opening activity of dihydropyridine ZM244085: effect on 86Rb efflux and 3H-P1075 binding in urinary bladder smooth muscle.

Trivedi S, Potter-Lee L, McConville MW, Li JH, Ohnmacht CJ, Trainor DA, Kau ST. Trivedi S, et al. Among authors: ohnmacht cj. Res Commun Mol Pathol Pharmacol. 1995 May;88(2):137-51. Res Commun Mol Pathol Pharmacol. 1995. PMID: 7670846

7

Anilide tertiary carbinols: a novel series of K+ channel openers.

Grant TL, Ohnmacht CJ, Howe BB. Grant TL, et al. Among authors: ohnmacht cj. Trends Pharmacol Sci. 1994 Nov;15(11):402-4. doi: 10.1016/0165-6147(94)90082-5. Trends Pharmacol Sci. 1994. PMID: 7855900 Review. No abstract available.

8

Studies of the K(ATP) channel opening activity of the new dihydropyridine compound 9-(3-cyanophenyl)-3,4,6,7,9,10-hexahydro-1,8-(2H,5H)-acridined ione in bladder detrusor in vitro.

Li JH, Yasay GD, Kau ST, Ohnmacht CJ, Trainor DA, Bonev AD, Heppner TJ, Nelson MT. Li JH, et al. Among authors: ohnmacht cj. Arzneimittelforschung. 1996 May;46(5):525-30. Arzneimittelforschung. 1996. PMID: 8737640

9

Pharmacological characterization of ZD6021: a novel, orally active antagonist of the tachykinin receptors.

Rumsey WL, Aharony D, Bialecki RA, Abbott BM, Barthlow HG, Caccese R, Ghanekar S, Lengel D, McCarthy M, Wenrich B, Undem B, Ohnmacht C, Shenvi A, Albert JS, Brown F, Bernstein PR, Russell K. Rumsey WL, et al. J Pharmacol Exp Ther. 2001 Jul;298(1):307-15. J Pharmacol Exp Ther. 2001. PMID: 11408556

10

Structural analysis and optimization of NK(1) receptor antagonists through modulation of atropisomer interconversion properties.

Albert JS, Ohnmacht C, Bernstein PR, Rumsey WL, Aharony D, Alelyunas Y, Russell DJ, Potts W, Sherwood SA, Shen L, Dedinas RF, Palmer WE, Russell K. Albert JS, et al. J Med Chem. 2004 Jan 29;47(3):519-29. doi: 10.1021/jm030197g. J Med Chem. 2004. PMID: 14736234

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