Duffy RA - Search Results

1

[3H]SCH 39166, a new D1-selective radioligand: in vitro and in vivo binding analyses.

McQuade RD, Duffy RA, Anderson CC, Crosby G, Coffin VL, Chipkin RE, Barnett A. McQuade RD, et al. Among authors: duffy ra. J Neurochem. 1991 Dec;57(6):2001-10. doi: 10.1111/j.1471-4159.1991.tb06415.x. J Neurochem. 1991. PMID: 1834801

2

In vivo binding to dopamine receptors: a correlate of potential antipsychotic activity.

McQuade RD, Duffy RA, Coffin VL, Barnett A. McQuade RD, et al. Among authors: duffy ra. Eur J Pharmacol. 1992 Apr 29;215(1):29-34. doi: 10.1016/0014-2999(92)90604-3. Eur J Pharmacol. 1992. PMID: 1355442

3

Selective up-regulation of D-1 dopamine receptors following chronic administration of SCH 39166 in primates.

Duffy RA, Kaminska G, Chipkin RE, McQuade RD. Duffy RA, et al. Pharmacol Biochem Behav. 1992 Jan;41(1):235-8. doi: 10.1016/0091-3057(92)90089-x. Pharmacol Biochem Behav. 1992. PMID: 1531704

4

In vivo binding of SCH 39166: a D-1 selective antagonist.

McQuade RD, Duffy RA, Coffin VL, Chipkin RE, Barnett A. McQuade RD, et al. Among authors: duffy ra. J Pharmacol Exp Ther. 1991 Apr;257(1):42-9. J Pharmacol Exp Ther. 1991. PMID: 1826927

5

Serotonergic component of SCH 23390: in vitro and in vivo binding analyses.

McQuade RD, Ford D, Duffy RA, Chipkin RE, Iorio LC, Barnett A. McQuade RD, et al. Among authors: duffy ra. Life Sci. 1988;43(23):1861-9. doi: 10.1016/s0024-3205(88)80003-1. Life Sci. 1988. PMID: 2904635

6

Characterization of the binding of SCH 39166 to the five cloned dopamine receptor subtypes.

Tice MA, Hashemi T, Taylor LA, Duffy RA, McQuade RD. Tice MA, et al. Among authors: duffy ra. Pharmacol Biochem Behav. 1994 Nov;49(3):567-71. doi: 10.1016/0091-3057(94)90070-1. Pharmacol Biochem Behav. 1994. PMID: 7862709

7

In vivo autoradiography of [3H]SCH 39166 in rat brain: selective displacement by D1/D5 antagonists.

Duffy RA, Hunt MA, Wamsley JK, McQuade RD. Duffy RA, et al. J Chem Neuroanat. 2000 May;19(1):41-6. doi: 10.1016/s0891-0618(00)00045-4. J Chem Neuroanat. 2000. PMID: 10882836

8

Diphenylsulfone muscarinic antagonists: piperidine derivatives with high M2 selectivity and improved potency.

Billard W, Binch H, Bratzler K, Chen LY, Crosby G Jr, Duffy RA, Dugar S, Lachowicz J, McQuade R, Pushpavanam P, Ruperto VB, Taylor LA, Clader JW. Billard W, et al. Among authors: duffy ra. Bioorg Med Chem Lett. 2000 Oct 2;10(19):2209-12. doi: 10.1016/s0960-894x(00)00437-6. Bioorg Med Chem Lett. 2000. PMID: 11012031

9

Diphenyl sulfoxides as selective antagonists of the muscarinic M2 receptor.

Kozlowski JA, Lowe DB, Guzik HS, Zhou G, Ruperto VB, Duffy RA, McQuade R, Crosby G, Taylor LA, Billard W, Binch H, Lachowicz JE. Kozlowski JA, et al. Among authors: duffy ra. Bioorg Med Chem Lett. 2000 Oct 16;10(20):2255-7. doi: 10.1016/s0960-894x(00)00438-8. Bioorg Med Chem Lett. 2000. PMID: 11055332

10

Benzylidene ketal derivatives as M2 muscarinic receptor antagonists.

Boyle CD, Chackalamannil S, Chen LY, Dugar S, Pushpavanam P, Billard W, Binch H 3rd, Crosby G, Cohen-Williams M, Coffin VL, Duffy RA, Ruperto V, Lachowicz JE. Boyle CD, et al. Among authors: duffy ra. Bioorg Med Chem Lett. 2000 Dec 18;10(24):2727-30. doi: 10.1016/s0960-894x(00)00553-9. Bioorg Med Chem Lett. 2000. PMID: 11133078

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