Overview

  • Product name

    Pyrantel pamoate, antiparasitic agent
  • Description

    Broad spectrum antiparasitic agent.
  • Biological description

    Broad spectrum antiparasitic agent. Shows depolarizing effects at the neuromuscular junction in vivo. Orally active with low absorbance by host intestines.
  • Purity

    > 98%
  • CAS Number

    22204-24-6
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    1-Methyl-2-[(E)-2-thiophen-2-ylethenyl]-5,6-dihydro-4H-pyrimidinium 4-[(3-carboxy-2-hydroxynaphthalen-1-yl)methyl]-3-hydroxynaphthalene-2-carboxylate
  • Molecular weight

    594.69
  • Molecular formula

    C11H14N2S.C23H16O6
  • PubChem identifier

    5281033
  • Storage instructions

    Store at Room Temperature. The product can be stored for up to 12 months.
  • Handling

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    CN1CCCN=C1C=CC2=CC=CS2.C1=CC=C2C(=C1)C=C(C(=C2CC3=C(C(=CC4=CC=CC=C43)C(=O)O)O)O)C(=O)O
  • Source

    Synthetic

  • Research areas

References

This product has been referenced in:

  • Nielsen MK  et al. Characterization of the inflammatory response to anthelmintic treatment of ponies with cyathostominosis. Vet J : (2013). Read more (PubMed: 24035469) »
  • Reinemeyer CR  et al. Efficacy of pyrantel pamoate and ivermectin paste formulations against naturally acquired Oxyuris equi infections in horses. Vet Parasitol 171:106-10 (2010). Read more (PubMed: 20307935) »
  • Ganguly B  et al. Regulation of cholinomimetic action of pyrantel pamoate by calcium channels in Setaria cervi. Indian J Physiol Pharmacol 40:245-8 (1996). Read more (PubMed: 8950141) »

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