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pubmed-article:14698167pubmed:abstractTextThiourea derivatives were identified as glyburide-reversible potassium channel openers through high-throughput screening. Based on these findings, a number of novel cyanoguanidines were designed and synthesized, which hyperpolarized human bladder K(ATP) channels. These agents are potent full agonists in relaxing electrically-stimulated pig bladder strips. The synthesis, SAR and biological properties of these agents are discussed.lld:pubmed
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pubmed-article:14698167pubmed:articleTitleDesign and synthesis of novel cyanoguanidine ATP-sensitive potassium channel openers for the treatment of overactive bladder.lld:pubmed
pubmed-article:14698167pubmed:affiliationAbbott Laboratories, Neuroscience Research, Global Pharmaceutical Research and Development, Abbott Park, IL 60064, USA. arturo.perezmedrano@abbott.comlld:pubmed
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