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2000 | 2 |
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Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 2. Selective and potent benzylamino cyclobutenediones.
J Med Chem. 2000 Mar 23;43(6):1203-14. doi: 10.1021/jm9905108.
J Med Chem. 2000.
PMID: 10737753
Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 1. N-Cyanoguanidine bioisosteres possessing in vivo bladder selectivity.
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.
Butera JA, et al. Among authors: antane mm.
J Med Chem. 2000 Mar 23;43(6):1187-202. doi: 10.1021/jm9905099.
J Med Chem. 2000.
PMID: 10737752
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Comparison of the potassium channel openers, WAY-133537, ZD6169, and celikalim on isolated bladder tissue and In vivo bladder instability in rat.
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.
Wojdan A, et al. Among authors: antane mm.
J Pharmacol Exp Ther. 1999 Jun;289(3):1410-8.
J Pharmacol Exp Ther. 1999.
PMID: 10336534
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