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Results: 1-7 |
Results: 7
New selective cytotoxic diterpenylquinones and diterpenylhydroquinones
Authors: del Corral, JMM Gordaliza, M Castro, MA Mahiques, MM Chamorro, P Molinari, A Garcia-Gravalos, MD Broughton, HB San Feliciano, A
Citation: Jmm. Del Corral et al., New selective cytotoxic diterpenylquinones and diterpenylhydroquinones, J MED CHEM, 44(8), 2001, pp. 1257-1267
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
Modified CoMFA methods for the analysis of antineoplastic effects of lignan analogues
Authors: Broughton, HB Gordaliza, M Castro, MA del Corral, JMM San Feliciano, A
Citation: Hb. Broughton et al., Modified CoMFA methods for the analysis of antineoplastic effects of lignan analogues, J MOL ST-TH, 504, 2000, pp. 287-294
Development of peptide 3D structure mimetics: Rational design of novel peptoid cholecystokinin receptor antagonists
Authors: Low, CMR Black, JW Broughton, HB Buck, IM Davies, JMR Dunstone, DJ Hull, RAD Kalindjian, SB McDonald, IM Pether, MJ Shankley, NP Steel, KIM
Citation: Cmr. Low et al., Development of peptide 3D structure mimetics: Rational design of novel peptoid cholecystokinin receptor antagonists, J MED CHEM, 43(19), 2000, pp. 3505-3517
Towards the synthesis of 9,11-secospongianes
Authors: Basabe, P Gomez, A Marcos, IS Martin, DD Broughton, HB Urones, JG
Citation: P. Basabe et al., Towards the synthesis of 9,11-secospongianes, TETRAHEDR L, 40(37), 1999, pp. 6857-6860
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: 1-7 |