Prisinzano TE - Search Results

1

Synthetic studies of neoclerodane diterpenes from Salvia divinorum: selective modification of the furan ring.

Harding WW, Schmidt M, Tidgewell K, Kannan P, Holden KG, Dersch CM, Rothman RB, Prisinzano TE. Harding WW, et al. Among authors: prisinzano te. Bioorg Med Chem Lett. 2006 Jun 15;16(12):3170-4. doi: 10.1016/j.bmcl.2006.03.062. Epub 2006 Apr 18. Bioorg Med Chem Lett. 2006. PMID: 16621556

2

Synthesis and Pharmacological Evaluation of Enantiopure N-Substituted Ortho-c Oxide-Bridged 5-Phenylmorphans.

Li F, Kopajtic TA, Katz JL, Luo D, Prisinzano TE, Imler GH, Deschamps JR, Jacobson AE, Rice KC. Li F, et al. Among authors: prisinzano te. Molecules. 2022 Dec 12;27(24):8808. doi: 10.3390/molecules27248808. Molecules. 2022. PMID: 36557961 Free PMC article.

3

Benzylimidazolines as h5-HT1B/1D serotonin receptor ligands: a structure-affinity investigation.

Law H, Dukat M, Teitler M, Lee DK, Mazzocco L, Kamboj R, Rampersad V, Prisinzano T, Glennon RA. Law H, et al. J Med Chem. 1998 Jun 18;41(13):2243-51. doi: 10.1021/jm970513p. J Med Chem. 1998. PMID: 9632357

4

Imidazoline-modified benzylimidazolines as h5-HT(1D/1B) serotonergic ligands.

Prisinzano T, Law H, Dukat M, Slassi A, MaClean N, Demchyshyn L, Glennon RA. Prisinzano T, et al. Bioorg Med Chem. 2001 Mar;9(3):613-9. doi: 10.1016/s0968-0896(00)00275-3. Bioorg Med Chem. 2001. PMID: 11310595

5

Synthesis and biological activity of 8beta-substituted hydrocodone indole and hydromorphone indole derivatives.

Yu H, Prisinzano T, Dersch CM, Marcus J, Rothman RB, Jacobson AE, Rice KC. Yu H, et al. Bioorg Med Chem Lett. 2002 Jan 21;12(2):165-8. doi: 10.1016/s0960-894x(01)00689-8. Bioorg Med Chem Lett. 2002. PMID: 11755345

6

Piperidine analogues of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine (GBR 12909): high affinity ligands for the dopamine transporter.

Prisinzano T, Greiner E, Johnson EM 2nd, Dersch CM, Marcus J, Partilla JS, Rothman RB, Jacobson AE, Rice KC. Prisinzano T, et al. J Med Chem. 2002 Sep 12;45(19):4371-4. doi: 10.1021/jm020264r. J Med Chem. 2002. PMID: 12213078

7

Synthesis and dopamine transporter affinity of chiral 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(2-hydroxypropyl)piperazines as potential cocaine abuse therapeutic agents.

Hsin LW, Prisinzano T, Wilkerson CR, Dersch CM, Horel R, Jacobson AE, Rothman RB, Rice KC. Hsin LW, et al. Bioorg Med Chem Lett. 2003 Feb 10;13(3):553-6. doi: 10.1016/s0960-894x(02)00940-x. Bioorg Med Chem Lett. 2003. PMID: 12565970

8

Further exploration of 1-[2-[Bis-(4-fluorophenyl)methoxy]ethyl]piperazine (GBR 12909): role of N-aromatic, N-heteroaromatic, and 3-oxygenated N-phenylpropyl substituents on affinity for the dopamine and serotonin transporter.

Lewis D, Zhang Y, Prisinzano T, Dersch CM, Rothman RB, Jacobson AE, Rice KC. Lewis D, et al. Bioorg Med Chem Lett. 2003 Apr 7;13(7):1385-9. doi: 10.1016/s0960-894x(03)00108-2. Bioorg Med Chem Lett. 2003. PMID: 12657288

9

Structure-activity relationship studies of highly selective inhibitors of the dopamine transporter: N-benzylpiperidine analogues of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine.

Greiner E, Prisinzano T, Johnson EM 2nd, Dersch CM, Marcus J, Partilla JS, Rothman RB, Jacobson AE, Rice KC. Greiner E, et al. J Med Chem. 2003 Apr 10;46(8):1465-9. doi: 10.1021/jm020419v. J Med Chem. 2003. PMID: 12672246

10

High-dose fenfluramine administration decreases serotonin transporter binding, but not serotonin transporter protein levels, in rat forebrain.

Rothman RB, Jayanthi S, Wang X, Dersch CM, Cadet JL, Prisinzano T, Rice KC, Baumann MH. Rothman RB, et al. Synapse. 2003 Dec 1;50(3):233-9. doi: 10.1002/syn.10266. Synapse. 2003. PMID: 14515341

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