Unelius L - Search Results

1

Derivatives of (R)-1,11-methyleneaporphine: synthesis, structure, and interactions with G-protein coupled receptors.

Linnanen T, Brisander M, Unelius L, Sundholm G, Hacksell U, Johansson AM. Linnanen T, et al. Among authors: unelius l. J Med Chem. 2000 Apr 6;43(7):1339-49. doi: 10.1021/jm9911433. J Med Chem. 2000. PMID: 10753471

2

Novel derivatives of 3-(dipropylamino)chroman. Interactions with 5-HT1A and D2A receptors.

Caldirola P, Chowdhury R, Unelius L, Mohell N, Hacksell U, Johansson AM. Caldirola P, et al. Among authors: unelius l. Bioorg Med Chem Lett. 1999 Jun 7;9(11):1583-6. doi: 10.1016/s0960-894x(99)00232-2. Bioorg Med Chem Lett. 1999. PMID: 10386940

3

Atropisomeric derivatives of 2',6'-disubstituted (R)-11-phenylaporphine: selective serotonin 5-HT(7) receptor antagonists.

Linnanen T, Brisander M, Unelius L, Rosqvist S, Nordvall G, Hacksell U, Johansson AM. Linnanen T, et al. Among authors: unelius l. J Med Chem. 2001 Apr 26;44(9):1337-40. doi: 10.1021/jm0108505. J Med Chem. 2001. PMID: 11311055 No abstract available.

4

(R)-11-hydroxy- and (R)-11-hydroxy-10-methylaporphine: synthesis, pharmacology, and modeling of D2A and 5-HT1A receptor interactions.

Hedberg MH, Johansson AM, Nordvall G, Yliniemelä A, Li HB, Martin AR, Hjorth S, Unelius L, Sundell S, Hacksell U. Hedberg MH, et al. Among authors: unelius l. J Med Chem. 1995 Feb 17;38(4):647-58. doi: 10.1021/jm00004a011. J Med Chem. 1995. PMID: 7861413

5

10-substituted 11-oxygenated (R)-aporphines: synthesis, pharmacology, and modeling of 5-HT1A receptor interactions.

Hedberg MH, Jansen JM, Nordvall G, Hjorth S, Unelius L, Johansson AM. Hedberg MH, et al. Among authors: unelius l. J Med Chem. 1996 Aug 30;39(18):3491-502. doi: 10.1021/jm960188q. J Med Chem. 1996. PMID: 8784447

6

11-substituted (R)-aporphines: synthesis, pharmacology, and modeling of D2A and 5-HT1A receptor interactions.

Hedberg MH, Linnanen T, Jansen JM, Nordvall G, Hjorth S, Unelius L, Johansson AM. Hedberg MH, et al. Among authors: unelius l. J Med Chem. 1996 Aug 30;39(18):3503-13. doi: 10.1021/jm960189i. J Med Chem. 1996. PMID: 8784448

7

Phenylpiperazine derivatives with strong affinity for 5HT1A, D2A and D3 receptors.

Terán C, Santana L, Uriarte E, Fall Y, Unelius L, Tolf BR. Terán C, et al. Among authors: unelius l. Bioorg Med Chem Lett. 1998 Dec 15;8(24):3567-70. doi: 10.1016/s0960-894x(98)00646-5. Bioorg Med Chem Lett. 1998. PMID: 9934472

8

Structural analogues of 5-OMe-BPAT: synthesis and interactions with dopamine D2, D3, and serotonin 5-HT1A receptors.

Homan EJ, Kroodsma E, Copinga S, Unelius L, Mohell N, Wikström HV, Grol CJ. Homan EJ, et al. Among authors: unelius l. Bioorg Med Chem. 1999 Jun;7(6):1111-21. doi: 10.1016/s0968-0896(99)00039-5. Bioorg Med Chem. 1999. PMID: 10428381

9

2-aminotetralin-derived substituted benzamides with mixed dopamine D2, D3, and serotonin 5-HT1A receptor binding properties: a novel class of potential atypical antipsychotic agents.

Homan EJ, Copinga S, Elfström L, van der Veen T, Hallema JP, Mohell N, Unelius L, Johansson R, Wikström HV, Grol CJ. Homan EJ, et al. Among authors: unelius l. Bioorg Med Chem. 1998 Nov;6(11):2111-26. doi: 10.1016/s0968-0896(98)00167-9. Bioorg Med Chem. 1998. PMID: 9881101

10

Synthesis and Pharmacology of the enantiomers of the potential atypical antipsychotic agents 5-OMe-BPAT and 5-OMe-(2,6-di-OMe)-BPAT.

Homan EJ, Copinga S, Unelius L, Jackson DM, Wikström HV, Grol CJ. Homan EJ, et al. Among authors: unelius l. Bioorg Med Chem. 1999 Jul;7(7):1263-71. doi: 10.1016/s0968-0896(99)00073-5. Bioorg Med Chem. 1999. PMID: 10465402

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