Imidafenacin (KRP-197, ONO-8025) is an orally active inhibitor of muscarinic (mAChR) M1 and M3 receptors. Imidafenacin potently inhibits bladder contraction in vivo and exerts an antidiuretic effect by enhancing the signaling pathway of vasopressin (antidiuretic hormone). Imidafenacin can be used in research related to overactive bladder[1][2].
Molecular Weight:
319.40
Purity:
99.26
CAS Number:
[170105-16-5]
Formula:
C20H21N3O
Target:
mAChR,Vasopressin Receptor
Application Notes:
MCE Product type: Reference compound
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