ChemSpider 2D Image | Zamifenacin fumarate | C31H33NO7

Zamifenacin fumarate

  • Molecular FormulaC31H33NO7
  • Average mass531.596 Da
  • Monoisotopic mass531.225708 Da
  • ChemSpider ID16741028
  • Double-bond stereo - Double-bond stereo

    defined stereocentres - 1 of 1 defined stereocentres


More details:






Validated by Experts, Validated by Users, Non-Validated, Removed by Users

(2E)-2-Butendisäure --(3R)-1-[2-(1,3-benzodioxol-5-yl)ethyl]-3-(diphenylmethoxy)piperidin (1:1) [German] [ACD/IUPAC Name]
(3R)-1-[2-(1,3-Benzodioxol-5-yl)ethyl]-3-(diphenylmethoxy)piperidine (2E)-2-butenedioate (1:1) [ACD/IUPAC Name]
(3R)-1-[2-(1,3-Benzodioxol-5-yl)ethyl]-3-(diphenylmethoxy)piperidine (2E)-but-2-enedioate (1:1)
127308-98-9 [RN]
Acide (2E)-2-butènedioïque - (3R)-1-[2-(1,3-benzodioxol-5-yl)éthyl]-3-(diphénylméthoxy)pipéridine (1:1) [French] [ACD/IUPAC Name]
Piperidine, 1-[2-(1,3-benzodioxol-5-yl)ethyl]-3-(diphenylmethoxy)-, (3R)-, (2E)-2-butenedioate (1:1) [ACD/Index Name]
Zamifenacin fumarate
(2E)-but-2-enedioic acid; (3R)-1-[2-(2H-1,3-benzodioxol-5-yl)ethyl]-3-(diphenylmethoxy)piperidine
(3R)-1-[2-(1-,3-Benzodioxol-5-yl)ethyl]-3-(diphenylmethoxy)piperidine fumarate
(3R)-1-[2-(1,3-benzodioxol-5-yl)ethyl]-3-(diphenylmethoxy)-piperidine, (2E)-2-butenedioate
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

UK 76654-2 {Fumarate} [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous
    • Bio Activity:

      7-TM Receptors Tocris Bioscience 2579
      Acetylcholine (Muscarinic) Receptors Tocris Bioscience 2579
      Acetylcholine Muscarinic Receptors Tocris Bioscience 2579
      M3 Receptors Tocris Bioscience 2579
      Selective M3 antagonist Tocris Bioscience 2579
      Selective M3 muscarinic receptor antagonist (pKi values are 8.52, 7.93, 7.90 and 7.78 for M3, M2, M1 and M4 receptors respectively). Displays higher affinity at ileal M3 receptors (pKi = 9.3) compared to oesophageal and tracheal M3 receptors (pKi values are 8.8 and 8.2 respectively). Inhibits gastrointestinal motility in vivo in the absence of cardiovascular effects. Tocris Bioscience 2579
      Selective M3 muscarinic receptor antagonist (pKi values are 8.52, 7.93, 7.90 and 7.78 for M3, M2, M1 and M4 receptors respectively). Displays higher affinity at ileal M3 receptors (pKi = 9.3) compared to oesophageal and tracheal M3 receptors (pKi values are 8.8 and 8.2 respectively). Inhibits gastrointestinal motility in vivo in the absence of cardiovascular effects. Tocris Bioscience 2579

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

No predicted properties have been calculated for this compound.

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