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Diclazuril

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Diclazuril
Clinical data
Trade namesCoxiril, Vecoxan
AHFS/Drugs.comInternational Drug Names
ATCvet code
Identifiers
  • 2-(4-Chlorophenyl)-2-[2,6-dichloro-4-(3,5-dioxo-1,2,4-triazin-2-yl)phenyl]acetonitrile
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.168.055Edit this at Wikidata
Chemical and physical data
FormulaC17H9Cl3N4O2
Molar mass407.64 g·mol−1
3D model (JSmol)
  • C1=CC(=CC=C1C(C#N)C2=C(C=C(C=C2Cl)N3C(=O)NC(=O)C=N3)Cl)Cl
  • InChI=1S/C17H9Cl3N4O2/c18-10-3-1-9(2-4-10)12(7-21)16-13(19)5-11(6-14(16)20)24-17(26)23-15(25)8-22-24/h1-6,8,12H,(H,23,25,26) ☒N
  • Key:ZSZFUDFOPOMEET-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Diclazuril (trade nameVecoxan) is acoccidiostat.[1] In 2025 diclazuril has also been reported to interact withtubulin and inhibit its polymerization.[2]


See also

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References

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  1. ^Diaferia M, Veronesi F, Morganti G, Nisoli L, Fioretti DP (August 2013)."Efficacy of toltrazuril 5 % suspension (Baycox®, Bayer) and diclazuril (Vecoxan®, Janssen-Cilag) in the control of Eimeria spp. in lambs".Parasitology Research.112 (Suppl 1):163–8.doi:10.1007/s00436-013-3440-1.PMID 23756962.
  2. ^Baksheeva VE, La Rocca R, Allegro D, Derviaux C, Pasquier E, Roche P, Morelli X, Devred F, Golovin AV, Tsvetkov PO (2025). "NanoDSF Screening for Anti-tubulin Agents Uncovers New Structure–Activity Insights".Journal of Medicinal Chemistry.doi:10.1021/acs.jmedchem.5c01008.
CARTooltip Constitutive androstane receptor
PXRTooltip Pregnane X receptor
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