Authors:
Baudy, RB
Fletcher, H
Yardley, JP
Zaleska, MM
Bramlett, DR
Tasse, RP
Kowal, DM
Katz, AH
Moyer, JA
Abou-Gharbia, M
Citation: Rb. Baudy et al., Design, synthesis, SAR, and biological evaluation of highly potent benzimidazole-spaced phosphono-alpha-amino acid competitive NMDA antagonists of the AP-6 type, J MED CHEM, 44(10), 2001, pp. 1516-1529
Authors:
Bartolomeo, AC
Morris, H
Buccafusco, JJ
Kille, N
Rosenzweig-Lipson, S
Husbands, MG
Sabb, AL
Abou-Gharbia, M
Moyer, JA
Boast, CA
Citation: Ac. Bartolomeo et al., The preclinical pharmacological profile of WAY-132983, a potent M1 preferring agonist, J PHARM EXP, 292(2), 2000, pp. 584-596
Authors:
Sabb, AL
Husbands, GM
Tokolics, J
Stein, RP
Tasse, RP
Boast, CA
Moyer, JA
Abou-Gharbia, M
Citation: Al. Sabb et al., Discovery of a highly potent, functionally-selective muscarinic M-1 agonist,WAY-132983 using rational drug design and receptor modelling, BIOORG MED, 9(14), 1999, pp. 1895-1900
Authors:
Abou-Gharbia, MA
Childers, WE
Fletcher, H
McGaughey, G
Patel, U
Webb, MB
Yardley, J
Andree, T
Boast, C
Kucharik, RJ
Marquis, K
Morris, H
Scerni, R
Moyer, JA
Citation: Ma. Abou-gharbia et al., Synthesis and SAR of adatanserin: Novel adamantyl aryl- and heteroarylpiperazines with dual serotonin 5-HT1A and 5-HT2 activity as potential anxiolytic and antidepressant agents, J MED CHEM, 42(25), 1999, pp. 5077-5094