AAAAAA

   
Results: 1-8 |
Results: 8
N-arylsulfonylindole derivatives as serotonin 5-HT6 receptor ligands
Authors: Russell, MGN Baker, RJ Barden, L Beer, MS Bristow, L Broughton, HB Knowles, M McAllister, G Patel, S Castro, JL
Citation: Mgn. Russell et al., N-arylsulfonylindole derivatives as serotonin 5-HT6 receptor ligands, J MED CHEM, 44(23), 2001, pp. 3881-3895
Analgesic and toxic effects of ABT-594 resemble epibatidine and nicotine in rats
Authors: Boyce, S Webb, JK Shepheard, SL Russell, MGN Hill, RG Rupniak, NMJ
Citation: S. Boyce et al., Analgesic and toxic effects of ABT-594 resemble epibatidine and nicotine in rats, PAIN, 85(3), 2000, pp. 443-450
Asymmetric synthesis of the northern segment of ephedradine C
Authors: Russell, MGN Baker, R Ball, RG Thomas, SR Tsou, NN Castro, JL
Citation: Mgn. Russell et al., Asymmetric synthesis of the northern segment of ephedradine C, J CHEM S P1, (6), 2000, pp. 893-899
Modulation of [H-3]MK-801 binding to NMDA receptors in vivo and in vitro
Authors: Murray, F Kennedy, J Hutson, PH Elliot, J Huscroft, I Mohnen, K Russell, MGN Grimwood, S
Citation: F. Murray et al., Modulation of [H-3]MK-801 binding to NMDA receptors in vivo and in vitro, EUR J PHARM, 397(2-3), 2000, pp. 263-270
2,7-Diazabicyclo[3.3.0]octanes as novel h5-HT1D receptor agonists
Authors: Russell, MGN Beer, MS Stanton, JA Sohal, B Mortishire-Smith, RJ Castro, JL
Citation: Mgn. Russell et al., 2,7-Diazabicyclo[3.3.0]octanes as novel h5-HT1D receptor agonists, BIOORG MED, 9(17), 1999, pp. 2491-2496
Asymmetric synthesis of the northern segment of ephedradine C. A novel dihydrobenzo[b]furan formation
Authors: Russell, MGN Baker, R Castro, JL
Citation: Mgn. Russell et al., Asymmetric synthesis of the northern segment of ephedradine C. A novel dihydrobenzo[b]furan formation, TETRAHEDR L, 40(49), 1999, pp. 8667-8670
3-[3-(Piperidin-1-yl)propyl] indoles as highly selective h5-HT1D receptor agonists
Authors: Russell, MGN Matassa, VG Pengilley, RR van Niel, MB Sohal, B Watt, AP Hitzel, L Beer, MS Stanton, JA Broughton, HB Castro, JL
Citation: Mgn. Russell et al., 3-[3-(Piperidin-1-yl)propyl] indoles as highly selective h5-HT1D receptor agonists, J MED CHEM, 42(24), 1999, pp. 4981-5001
Fluorination of 3-(3-(piperidin-1-yl)propyl)indoles and 3-(3-(piperazin-1-yl)propyl)indoles gives selective human 5-HT1D receptor ligands with improved pharmacokinetic profiles
Authors: van Niel, MB Collins, I Beer, MS Broughton, HB Cheng, SKF Goodacre, SC Heald, A Locker, KL MacLeod, AM Morrison, D Moyes, CR O'Connor, D Pike, A Rowley, M Russell, MGN Moyes, CR O'Connor, D Pike, A Rowley, M Russell, MGN Sohal, B Stanton, JA Thomas, S Verrier, H Watt, AP Castro, JL
Citation: Mb. Van Niel et al., Fluorination of 3-(3-(piperidin-1-yl)propyl)indoles and 3-(3-(piperazin-1-yl)propyl)indoles gives selective human 5-HT1D receptor ligands with improved pharmacokinetic profiles, J MED CHEM, 42(12), 1999, pp. 2087-2104
Risultati: 1-8 |