Authors:
Poon, GK
Chen, Q
Teffera, Y
Ngui, JS
Griffin, PR
Braun, MP
Doss, GA
Freeden, C
Stearns, RA
Evans, DC
Baillie, TA
Tang, W
Citation: Gk. Poon et al., Bioactivation of diclofenac via benzoquinone imine intermediates-identification of urinary mercapturic acid derivatives in rats and humans, DRUG META D, 29(12), 2001, pp. 1608-1613
Authors:
Butera, JA
Antane, MM
Antane, SA
Argentieri, TM
Freeden, C
Graceffa, RF
Hirth, BH
Jenkins, D
Lennox, JR
Matelan, E
Norton, NW
Quagliato, D
Sheldon, JH
Spinelli, W
Warga, D
Wojdan, A
Woods, M
Citation: Ja. Butera et al., Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 1. N-cyanoguanidine bioisosteres possessing in vivo bladderselectivity, J MED CHEM, 43(6), 2000, pp. 1187-1202
Authors:
Gilbert, AM
Antane, MM
Argentieri, TM
Butera, JA
Francisco, GD
Freeden, C
Gundersen, EC
Graceffa, RF
Herbst, D
Hirth, BH
Lennox, JR
McFarlane, G
Norton, NW
Quagliato, D
Sheldon, JH
Warga, D
Wojdan, A
Woods, M
Citation: Am. Gilbert et al., Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 2. Selective and potent benzylamino cyclobutenediones, J MED CHEM, 43(6), 2000, pp. 1203-1214
Authors:
Wojdan, A
Freeden, C
Woods, M
Oshiro, G
Spinelli, W
Colatsky, TJ
Sheldon, JH
Norton, NW
Warga, D
Antane, MM
Antane, SA
Butera, JA
Argentieri, TM
Citation: A. Wojdan et al., Comparison of the potassium channel openers, WAY-133537, ZD6169, and celikalim on isolated bladder tissue and in vivo bladder instability in rat, J PHARM EXP, 289(3), 1999, pp. 1410-1418