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ritobegron

Known as: (4-(2-(((1R,2S)-1-Hydroxy-1-(4-Hydroxyphenyl)Propan-2-Yl)Amino)Ethyl)-2,5-Dimethylphenoxy)Acetic Acid, 2-(4-(2-((2-hydroxy-2-(4-hydroxyphenyl)-1-methylethyl)amino)ethyl)-2,5-dimethylphenyloxy)acetic acid 
 
National Institutes of Health

Papers overview

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Review
2016
Review
2016
INTRODUCTION Drugs which prevent acetylcholine mediated involuntary detrusor contractions are the mainstay of overactive bladder… Expand
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2016
2016
We evaluated the effects of probenecid, a potent organic anion transporter 1 (OAT1) and OAT3 inhibitor, on the pharmacokinetics… Expand
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Review
2016
Review
2016
INTRODUCTION Urinary incontinence in men is a significant and often underappreciated problem. Men can have urgency and or stress… Expand
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Review
2015
Review
2015
INTRODUCTION Antimuscarinic drugs form the mainstay of medical treatment for Overactive bladder Syndrome (OAB). With a proven… Expand
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2015
2015
Ritobegron, a selective β3-adrenoceptor agonist, is the prodrug of the active compound, KUC-7322. We investigated species… Expand
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2014
2014
The pharmacokinetic profile of ritobegron, a novel, selective β3-adrenoceptor agonist, was investigated in rats. Ritobegron, an… Expand
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2014
2014
Chapter 6 Purpose: KUC-7322 is the active metabolite of ritobegron, a selective β 3 -adrenoceptor agonist in development for the… Expand
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2012
2012
We performed in vitro and in vivo experiments to evaluate the pharmacological profile of ritobegron and its effects on the… Expand
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2012
2012
We evaluated the pharmacological profile of ritobegron [KUC-7483; (-)-ethyl 2-[4-(2-{[(1S,2R)-2-hydroxy-2-(4-hydroxyphenyl)-1… Expand
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2012
2012
The objective of this study was to investigate the effects of the β3-adrenoceptor (AR) agonist ritobegron on rat bladder function… Expand
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