Neumeyer JL - 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: neumeyer jl. J Med Chem. 1990 Jan;33(1):39-44. doi: 10.1021/jm00163a007. J Med Chem. 1990. PMID: 2136919

2

Synthesis and neuropharmacological evaluation of R(-)-N-alkyl-11-hydroxynoraporphines and their esters.

Csutoras C, Zhang A, Zhang K, Kula NS, Baldessarini RJ, Neumeyer JL. Csutoras C, et al. Among authors: neumeyer jl. Bioorg Med Chem. 2004 Jul 1;12(13):3553-9. doi: 10.1016/j.bmc.2004.04.029. Bioorg Med Chem. 2004. PMID: 15186839

3

Synthesis and amine transporter affinities of novel phenyltropane derivatives as potential positron emission tomography (PET) imaging agents.

Peng X, Zhang A, Kula NS, Baldessarini RJ, Neumeyer JL. Peng X, et al. Among authors: neumeyer jl. Bioorg Med Chem Lett. 2004 Nov 15;14(22):5635-9. doi: 10.1016/j.bmcl.2004.08.049. Bioorg Med Chem Lett. 2004. PMID: 15482938

4

Synthesis and dopamine receptor binding of sulfur-containing aporphines.

Tóth M, Berényi S, Csutorás C, Kula NS, Zhang K, Baldessarini RJ, Neumeyer JL. Tóth M, et al. Among authors: neumeyer jl. Bioorg Med Chem. 2006 Mar 15;14(6):1918-23. doi: 10.1016/j.bmc.2005.10.049. Epub 2005 Nov 15. Bioorg Med Chem. 2006. PMID: 16290940

5

Synthesis and dopamine receptor affinities of N-alkyl-11-hydroxy-2-methoxynoraporphines: N-alkyl substituents determine D1 versus D2 receptor selectivity.

Si YG, Gardner MP, Tarazi FI, Baldessarini RJ, Neumeyer JL. Si YG, et al. Among authors: neumeyer jl. J Med Chem. 2008 Feb 28;51(4):983-7. doi: 10.1021/jm701045j. Epub 2008 Feb 6. J Med Chem. 2008. PMID: 18251489

6

Aporphines, 36. Dopamine receptor interactions of trihydroxyaporphines. Synthesis, radioreceptor binding, and striatal adenylate cyclase stimulation of 2,10,11-trihydroxyaporphines in comparison with other hydroxylated aporphines.

Neumeyer JL, Arana GW, Law SJ, Lamont JS, Kula NS, Baldessarini RJ. Neumeyer JL, et al. J Med Chem. 1981 Dec;24(12):1440-5. doi: 10.1021/jm00144a014. J Med Chem. 1981. PMID: 7310821

7

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. J Med Chem. 1994 May 27;37(11):1558-61. doi: 10.1021/jm00037a004. J Med Chem. 1994. PMID: 8201589 No abstract available.

8

N-substituted analogs of 2 beta-carbomethoxy-3 beta- (4'-iodophenyl)tropane (beta-CIT) with selective affinity to dopamine or serotonin transporters in rat forebrain.

Neumeyer JL, Tamagnan G, Wang S, Gao Y, Milius RA, Kula NS, Baldessarini RJ. Neumeyer JL, et al. J Med Chem. 1996 Jan 19;39(2):543-8. doi: 10.1021/jm9505324. J Med Chem. 1996. PMID: 8558525

9

Synthesis and biological evaluation of a series of novel N- or O-fluoroalkyl derivatives of tropane: potential positron emission tomography (PET) imaging agents for the dopamine transporter.

Gu XH, Zong R, Kula NS, Baldessarini RJ, Neumeyer JL. Gu XH, et al. Among authors: neumeyer jl. Bioorg Med Chem Lett. 2001 Dec 3;11(23):3049-53. doi: 10.1016/s0960-894x(01)00626-6. Bioorg Med Chem Lett. 2001. PMID: 11714608

10

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. J Recept Res. 1988;8(1-4):83-96. doi: 10.3109/10799898809048979. J Recept Res. 1988. PMID: 3385694

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