Triclabendazole Sulfoxide

For research use only. Not for therapeutic Use.

  • CAT Number: R042343
  • CAS Number: 100648-13-3
  • Molecular Formula: C14H9Cl3N2O2S
  • Molecular Weight: 375.65
  • Purity: ≥95%
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Triclabendazole Sulfoxide(Cat No.:R042343)is the active metabolite of triclabendazole, a benzimidazole derivative highly effective against liver flukes (Fasciola hepatica and Fasciola gigantica). It disrupts the parasite’s microtubule function and energy metabolism, leading to its paralysis and death. Triclabendazole Sulfoxide exhibits excellent efficacy against both immature and adult fluke stages, making it a preferred treatment for fascioliasis in livestock and humans. Its broad-spectrum activity and safety profile support its use in veterinary and clinical medicine, contributing significantly to parasitic disease management in endemic regions.


Catalog Number R042343
CAS Number 100648-13-3
Synonyms

6-Chloro-5-(2,3-dichlorophenoxy)-2-(methylsulfinyl)-1H-benzimidazole

Molecular Formula C14H9Cl3N2O2S
Purity ≥95%
Storage -20°C
Related CAS 109536-20-1;    
IUPAC Name 6-chloro-5-(2,3-dichlorophenoxy)-2-methylsulfinyl-1H-benzimidazole
InChI InChI=1S/C14H9Cl3N2O2S/c1-22(20)14-18-9-5-8(16)12(6-10(9)19-14)21-11-4-2-3-7(15)13(11)17/h2-6H,1H3,(H,18,19)
InChIKey GABQPFWIQFRJSE-UHFFFAOYSA-N
SMILES CS(=O)C1=NC2=CC(=C(C=C2N1)Cl)OC3=C(C(=CC=C3)Cl)Cl
Reference

<p>
<span style=”font-size:12px;”><span style=”font-family:arial,helvetica,sans-serif;”>1.<span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Dupuy, Jacques, et al. &quot;Interaction of anthelmintic drugs with P-glycoprotein in recombinant LLC-PK1-mdr1a cells.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Chemico-biological interactions</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;186.3 (2010): 280-286.<br />
2.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Mestorino, N., et al. &quot;Pharmacokinetic disposition of triclabendazole in cattle and sheep; discrimination of the order and the rate of the absorption process of its active metabolite triclabendazole sulfoxide.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Veterinary research communications</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;32.1 (2008): 21-33.<br />
3.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Barrera, Borja, et al. &quot;The anthelmintic triclabendazole and its metabolites inhibit the membrane transporter ABCG2/BCRP.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Antimicrobial agents and chemotherapy</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;56.7 (2012): 3535-3543.<br />
4.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Keiser, Jennifer, et al. &quot;Triclabendazole and its two main metabolites lack activity against Schistosoma mansoni in the mouse model.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>The American journal of tropical medicine and hygiene</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;75.2 (2006): 287-291.<br />
5.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Mestorino, N., et al. &quot;Pharmacokinetic disposition of triclabendazole in cattle and sheep; discrimination of the order and the rate of the absorption process of its active metabolite triclabendazole sulfoxide.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Veterinary research communications</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;32.1 (2008): 21-33.<br />
6.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Halferty, L., et al. &quot;Relative activity of triclabendazole metabolites against the liver fluke, Fasciola hepatica.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Veterinary parasitology</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;159.2 (2009): 126-138.</span></span></span></p>

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