Acotiamide

CAT:
804-HY-121467-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Acotiamide - image 1

Acotiamide

  • Product Name Alternative:

    Z-338 (free base); YM443 (free base)
  • UNSPSC Description:

    Acotiamide is an orally active, selective and reversible acetylcholinesterase (AChE) inhibitor, with an IC50 of 1.79 μM. Acotiamide can enhance gastric contractility and accelerate delayed gastric emptying. Acotiamide has the potential for the research of functional dyspepsia involving gastric motility dysfunction and intestinal inflammatory[1][2][3].
  • Target Antigen:

    Cholinesterase (ChE)
  • Type:

    Reference compound
  • Related Pathways:

    Neuronal Signaling
  • Field of Research:

    Metabolic Disease; Inflammation/Immunology
  • Assay Protocol:

    https://www.medchemexpress.com/acotiamide.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O=C(C1=CSC(NC(C2=CC(OC)=C(OC)C=C2O)=O)=N1)NCCN(C(C)C)C(C)C
  • Molecular Weight:

    450.55
  • References & Citations:

    [1]Kazuyoshi Y oshii, et al. Physiologically-Based Pharmacokinetic and Pharmacodynamic Modeling for the Inhibition of Acetylcholinesterase by Acotiamide, A Novel Gastroprokinetic Agent for the Treatment of Functional Dyspepsia, in Rat Stomach. Pharmaceutical Research, 33(2), 292–300.|[2]Hiroshi Yamawaki, et al. Acotiamide attenuates central urocortin 2-induced intestinal inflammatory responses, and urocortin 2 treatment reduces TNF-α productions in LPS-stimulated macrophage cell lines. Neurogastroenterol Motil. 2020 Aug;32(8):e13813.|[3]Matsunaga Y, Acotiamide hydrochloride (Z-338), a new selective acetylcholinesterase inhibitor, enhances gastric motility without prolonging QT interval in dogs: comparison with cisapride, itopride, and mosapride. J Pharmacol Exp Ther. 2011 Mar;336(3):791-800.
  • Shipping Conditions:

    Room temperature
  • Clinical Information:

    Launched
  • CAS Number:

    185106-16-5