Wikström H - Search Results

1

Inhibition of lipid peroxidation mediated by indolizines.

Nasir AI, Gundersen LL, Rise F, Antonsen O, Kristensen T, Langhelle B, Bast A, Custers I, Haenen GR, Wikström H. Nasir AI, et al. Among authors: wikstrom h. Bioorg Med Chem Lett. 1998 Jul 21;8(14):1829-32. doi: 10.1016/s0960-894x(98)00313-8. Bioorg Med Chem Lett. 1998. PMID: 9873442

2

Thiazoloindans and thiazolobenzopyrans: a novel class of orally active central dopamine (partial) agonists.

van Vliet LA, Rodenhuis N, Wikström H, Pugsley TA, Serpa KA, Meltzer LT, Heffner TG, Wise LD, Lajiness ME, Huff RM, Svensson K, Haenen GR, Bast A. van Vliet LA, et al. Among authors: wikstrom h. J Med Chem. 2000 Sep 21;43(19):3549-57. doi: 10.1021/jm000087z. J Med Chem. 2000. PMID: 11000009

3

C5-substituted derivatives of 5-OMe-BPAT: synthesis and interactions with dopamine D2 and serotonin 5-HT1A receptors.

Homan EJ, Tulp MT, Nilsson JE, Wikström HV, Grol CJ. Homan EJ, et al. Among authors: wikstrom hv. Bioorg Med Chem. 1999 Nov;7(11):2541-8. doi: 10.1016/s0968-0896(99)00196-0. Bioorg Med Chem. 1999. PMID: 10632064

4

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: wikstrom hv. Bioorg Med Chem. 1998 Nov;6(11):2111-26. doi: 10.1016/s0968-0896(98)00167-9. Bioorg Med Chem. 1998. PMID: 9881101

5

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: wikstrom hv. Bioorg Med Chem. 1999 Jun;7(6):1111-21. doi: 10.1016/s0968-0896(99)00039-5. Bioorg Med Chem. 1999. PMID: 10428381

6

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: wikstrom hv. Bioorg Med Chem. 1999 Jul;7(7):1263-71. doi: 10.1016/s0968-0896(99)00073-5. Bioorg Med Chem. 1999. PMID: 10465402

7

Electrooxidation potential as a tool in the early screening for new safer clozapine-like analogues.

Mouithys-Mickalad A, Kauffmann JM, Petit C, Bruhwyler J, Liao Y, Wikström H, Damas J, Delarge J, Deby-Dupont G, Géczy J, Liégeois JF. Mouithys-Mickalad A, et al. Among authors: wikstrom h. J Med Chem. 2001 Mar 1;44(5):769-76. doi: 10.1021/jm000221f. J Med Chem. 2001. PMID: 11262087

8

Short and efficient syntheses of analogues of WAY-100635: new and potent 5-HT1A receptor antagonists.

Marchais S, Nowicki B, Wikström H, Brennum LT, Halldin C, Pike VW. Marchais S, et al. Among authors: wikstrom h. Bioorg Med Chem. 2001 Mar;9(3):695-702. doi: 10.1016/s0968-0896(00)00287-x. Bioorg Med Chem. 2001. PMID: 11310604

9

GRID/GOLPE 3D quantitative structure-activity relationship study on a set of benzamides and naphthamides, with affinity for the dopamine D3 receptor subtype.

Nilsson J, Wikström H, Smilde A, Glase S, Pugsley T, Cruciani G, Pastor M, Clementi S. Nilsson J, et al. Among authors: wikstrom h. J Med Chem. 1997 Mar 14;40(6):833-40. doi: 10.1021/jm9605952. J Med Chem. 1997. PMID: 9083471

10

5-(Sulfonyl)oxy-tryptamines and ethylamino side chain restricted derivatives. Structure-affinity relationships for h5-HT1B and h5-HT1D receptors.

Barf T, Wikström H, Pauwels PJ, Palmier C, Tardif S, Lundmark M, Sundell S. Barf T, et al. Among authors: wikstrom h. Bioorg Med Chem. 1998 Sep;6(9):1469-79. doi: 10.1016/s0968-0896(98)00079-0. Bioorg Med Chem. 1998. PMID: 9801818

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