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  • Adrenergic Receptor
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Results for "

human β3-adrenergic receptor

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    6
    TargetMol | Inhibitors_Agonists
LY377604
T15819204592-94-9In house
LY377604 is a human β3-adrenergic receptor agonist (EC50: 2.4 nM) and β1 2-adrenergic receptor antagonist for the study of obesity.
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6-8 weeks
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Ritobegron HCl
Ritobegron hydrochloride, KUC-7483, KUC7483, KUC 7483
T34333476333-91-2In house
Ritobegron (KUC-7483), an effective and selective β3-adrenergic receptor agonist, shows effective β(3)-AR agonist activity on transfected human β-AR and has an effect on the bladder of rats Shows high selectivity with other organs.
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3-6 months
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Solabegron
GW 427353
T12970252920-94-8
Solabegron (GW 427353) is a selective β3-adrenergic receptor agonist that promotes cAMP accumulation in Chinese hamster ovary cells expressing the human β3-AR (EC50: 22 nM). It is used to treat overactive bladder and irritable bowel syndrome.
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Ritobegron ethyl
Ritobegron ethyl, (-)-, KUC-7483 free base, (-)-Ritobegron ethyl
T202780255733-81-4
Ritobegron (also known as KUC-7483) is a potent and selective β3-adrenergic receptor agonist. In studies involving transfected human β-AR, Ritobegron exhibits significant and selective agonistic activity towards β(3)-AR. In rats, it shows high selectivity for the bladder over other organs. In anesthetized rats, Ritobegron effectively reduces bladder pressure with minimal impact on the cardiovascular system. It holds potential as a compound for treating overactive bladder.
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L-796568 free base
T24380211031-01-5
L-796568 free base is a β3 adrenergic receptor agonist potentially for the treatment of obesity. L-796568 is a potent full beta(3) agonist (EC50: 3.6 nM). It has 600-fold selectivity over the human beta(1) and beta(2) receptors.
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8-10 weeks
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L-796568 dihydrochloride
L 796568,L-796568,L796568
T27786211031-81-1
L-796568, is a β3 adrenergic receptor agonist. L-796568 is a potent full beta(3) agonist (EC(50) = 3.6 nM, 94% activation) with >600-fold selectivity over the human beta(1) and beta(2) receptors, which also displays good oral bioavailability in several
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8-10 weeks
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