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Results: 1-7 |
Results: 7
Serotonergic and dopaminergic activities of rigidified (R)-aporphine derivatives
Authors: Linnanen, T Brisander, M Mohell, N Johansson, AM
Citation: T. Linnanen et al., Serotonergic and dopaminergic activities of rigidified (R)-aporphine derivatives, BIOORG MED, 11(3), 2001, pp. 367-370
The pharmacological profile of (R)-3,4-dihydro-N-isopropyl-3-(N-isopropyl-N-propylamino)-2H-1-benzopyran-5-carboxamide, a selective 5-hydroxytryptamine(1A) receptor agonist
Authors: Renyi, L Evenden, JL Fowler, CJ Jerning, E Kelder, D Lake-Bakaar, D Larsson, LG Mohell, N Sallemark, M Ross, SB
Citation: L. Renyi et al., The pharmacological profile of (R)-3,4-dihydro-N-isopropyl-3-(N-isopropyl-N-propylamino)-2H-1-benzopyran-5-carboxamide, a selective 5-hydroxytryptamine(1A) receptor agonist, J PHARM EXP, 299(3), 2001, pp. 883-893
Site-directed mutagenesis of the 5-HT1B receptor increases the affinity of5-HT for the agonist low-affinity conformation and reduces the intrinsic activity of 5-HT
Authors: Granas, C Nordquist, J Mohell, N Larhammar, D
Citation: C. Granas et al., Site-directed mutagenesis of the 5-HT1B receptor increases the affinity of5-HT for the agonist low-affinity conformation and reduces the intrinsic activity of 5-HT, EUR J PHARM, 421(2), 2001, pp. 69-76
Synthesis of novel 5-substituted 3-amino-3,4-dihydro-2H-1-benzopyran derivatives and their interactions with the 5-HT1A receptor
Authors: Hammarberg, E Nordvall, G Leideborg, R Nylof, M Hanson, S Johansson, L Thorberg, SO Tolf, BR Jerning, E Svantesson, GT Mohell, N Ahlgren, C Westlind-Danielsson, A Csoregh, I Johansson, R
Citation: E. Hammarberg et al., Synthesis of novel 5-substituted 3-amino-3,4-dihydro-2H-1-benzopyran derivatives and their interactions with the 5-HT1A receptor, J MED CHEM, 43(15), 2000, pp. 2837-2850
Structural analogues of 5-OMe-BPAT: Synthesis and interactions with dopamine D-2, D-3, and serotonin 5-HT1A receptors
Authors: Homan, EJ Kroodsma, E Copinga, S Unelius, L Mohell, N Wikstrom, HV Grol, CJ
Citation: Ej. Homan et al., Structural analogues of 5-OMe-BPAT: Synthesis and interactions with dopamine D-2, D-3, and serotonin 5-HT1A receptors, BIO MED CH, 7(6), 1999, pp. 1111-1121
Novel derivatives of 3-(dipropylamino) chroman. Interactions with 5-HT1A and D-2A receptors.
Authors: Caldirola, P Chowdhury, R Unelius, L Mohell, N Hacksell, U Johansson, AM
Citation: P. Caldirola et al., Novel derivatives of 3-(dipropylamino) chroman. Interactions with 5-HT1A and D-2A receptors., BIOORG MED, 9(11), 1999, pp. 1583-1586
2-aminotetralin-derived substituted benzamides with mixed dopamine D-2, D-3, and serotonin 5-HT1A receptor binding properties: A novel class of potential atypical antipsychotic agents
Authors: Homan, EJ Copinga, S Elfstrom, L van der Veen, T Hallema, JP Mohell, N Unelius, L Johansson, R Wikstrom, HV Grol, CJ
Citation: Ej. Homan et al., 2-aminotetralin-derived substituted benzamides with mixed dopamine D-2, D-3, and serotonin 5-HT1A receptor binding properties: A novel class of potential atypical antipsychotic agents, BIO MED CH, 6(11), 1998, pp. 2111-2126
Risultati: 1-7 |