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imidafenacin

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    4
    TargetMol | Inhibitors_Agonists
  • Isotope Products
    1
    TargetMol | Isotope_Products
Imidafenacin
KRP-197, ONO-8025
T4986170105-16-5
Imidafenacin (KRP-197)(KRP-197; ONO-8025) is a potent and selective inhibitor of M3 receptors with Kb of 0.317 nM.
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Imidafenacin Metabolite M4
Imidafenacin Metabolite M4
T36662503598-17-2
Imidafenacin metabolite M4 is a metabolite of the muscarinic acetylcholine receptor antagonist imidafenacin.1It is formed from imidafenacin by the cytochrome P450 (CYP) isoform CYP3A4. 1.Kanayama, N., Kanari, C., Masuda, Y., et al.Drug-drug interactions in the metabolism of imidafenacin: Role of the human cytochrome P450 enzymes and UDP-glucuronic acid transferases, and potential of imidafenacin to inhibit human cytochrome P450 enzymesXenobiotica37(2)139-154(2007)
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Imidafenacin hydrochloride
ONO-8025 hydrochloride, KRP-197 hydrochloride
T86715893421-54-0
Imidafenacin hydrochloride is a highly effective and selective M3 receptor inhibitor with a Kb value of 0.317 nM [1].
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10-14 weeks
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Imidafenacin-d10
TMIJ-0336
Imidafenacin-d10 is a deuterated compound of Imidafenacin. Imidafenacin has a CAS number of 170105-16-5. Imidafenacin(KRP-197; ONO-8025) is a potent and selective inhibitor of M3 receptors with Kb of 0.317 nM.
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20 days
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