Campbell A - Search Results

1

Synthesis and structural requirements of N-substituted norapomorphines for affinity and activity at dopamine D-1, D-2, and agonist receptor sites in rat brain.

Gao YG, Ram VJ, Campbell A, Kula NS, Baldessarini RJ, Neumeyer JL. Gao YG, et al. Among authors: campbell a. J Med Chem. 1990 Jan;33(1):39-44. doi: 10.1021/jm00163a007. J Med Chem. 1990. PMID: 2136919

2

Prolonged D2 antidopaminergic activity of alkylating and nonalkylating derivatives of spiperone in rat brain.

Baldessarini RJ, Kula NS, Campbell A, Bakthavachalam V, Yuan J, Neumeyer JL. Baldessarini RJ, et al. Among authors: campbell a. Mol Pharmacol. 1992 Nov;42(5):856-63. Mol Pharmacol. 1992. PMID: 1435753

3

R(-)2-fluoro-N-n-propylnorapomorphine: a very potent and D2-selective dopamine agonist.

Baldessarini RJ, Kula NS, Gao Y, Campbell A, Neumeyer JL. Baldessarini RJ, et al. Among authors: campbell a. Neuropharmacology. 1991 Jan;30(1):97-9. doi: 10.1016/0028-3908(91)90049-h. Neuropharmacology. 1991. PMID: 1675452

4

R(-) and S(+) stereoisomers of 11-hydroxy- and 11-methoxy-N-n-propylnoraporphine: central dopaminergic behavioral activity in the rat.

Campbell A, Baldessarini RJ, Gao Y, Zong R, Neumeyer JL. Campbell A, et al. Neuropharmacology. 1990 Jun;29(6):527-36. doi: 10.1016/0028-3908(90)90064-x. Neuropharmacology. 1990. PMID: 1974710

5

Neuropharmacology and stereochemistry of dopamine receptor agonist and antagonist enantiomeric pairs.

Neumeyer JL, Froimowitz M, Baldessarini RJ, Campbell A, Gao YG. Neumeyer JL, et al. Among authors: campbell a. J Recept Res. 1988;8(1-4):83-96. doi: 10.3109/10799898809048979. J Recept Res. 1988. PMID: 3385694

6

Synthesis and dopamine agonist and antagonist effects of (R)-(-)- and (S)-(+)-11-hydroxy-N-n-propylnoraporphine.

Gao Y, Zong R, Campbell A, Kula NS, Baldessarini RJ, Neumeyer JL. Gao Y, et al. Among authors: campbell a. J Med Chem. 1988 Jul;31(7):1392-6. doi: 10.1021/jm00402a024. J Med Chem. 1988. PMID: 3385732

7

Aporphines. 48. Enantioselectivity of (R)-(-)- and (S)-(+)-N-n-propylnorapomorphine on dopamine receptors.

Neumeyer JL, Reischig D, Arana GW, Campbell A, Baldessarini RJ, Kula NS, Watling KJ. Neumeyer JL, et al. Among authors: campbell a. J Med Chem. 1983 Apr;26(4):516-21. doi: 10.1021/jm00358a011. J Med Chem. 1983. PMID: 6682147

8

N-omega-fluoroalkyl analogs of (1R)-2 beta-carbomethoxy-3 beta-(4-iodophenyl)-tropane (beta-CIT): radiotracers for positron emission tomography and single photon emission computed tomography imaging of dopamine transporters.

Neumeyer JL, Wang S, Gao Y, Milius RA, Kula NS, Campbell A, Baldessarini RJ, Zea-Ponce Y, Baldwin RM, Innis RB. Neumeyer JL, et al. Among authors: campbell a. J Med Chem. 1994 May 27;37(11):1558-61. doi: 10.1021/jm00037a004. J Med Chem. 1994. PMID: 8201589 No abstract available.

9

Inhibition of dopamine synthesis in rat striatal minces: evidence of dopamine autoreceptor supersensitivity to S(+)- but not R(-)-N-n-propylnorapomorphine after pretreatment with fluphenazine.

Booth RG, Baldessarini RJ, Campbell A. Booth RG, et al. Among authors: campbell a. Biochem Pharmacol. 1991 Jun 15;41(12):2040-3. doi: 10.1016/0006-2952(91)90148-x. Biochem Pharmacol. 1991. PMID: 1674873

10

Selective antidopaminergic effects of S(+)N-n-propylnoraporphines in limbic versus extrapyramidal sites in rat brain: comparisons with typical and atypical antipsychotic agents.

Campbell A, Yeghiayan S, Baldessarini RJ, Neumeyer JL. Campbell A, et al. Psychopharmacology (Berl). 1991;103(3):323-9. doi: 10.1007/BF02244285. Psychopharmacology (Berl). 1991. PMID: 1676180

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