Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 Mechanism of action  





2 Warnings  





3 References  














Pyriprole






العربية
Italiano
Српски / srpski
Srpskohrvatski / српскохрватски
 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 




In other projects  



Wikimedia Commons
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


Pyriprole
Ball-and-stick model of the pyriprole molecule
Clinical data
Trade namesPrac-tic
ATCvet code
Identifiers
  • 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(difluoromethyl)thio]-5-[(2-pyridinylmethyl)amino]-1H-pyrazole-3-carbonitrile

CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC18H10Cl2F5N5S
Molar mass494.27 g·mol−1
3D model (JSmol)
  • Clc2cc(C(F)(F)F)cc(Cl)c2-n(nc(C#N)c1SC(F)F)c1NCc3ncccc3

  • InChI=1S/C18H10Cl2F5N5S/c19-11-5-9(18(23,24)25)6-12(20)14(11)30-16(28-8-10-3-1-2-4-27-10)15(31-17(21)22)13(7-26)29-30/h1-6,17,28H,8H2 ☒N

  • Key:MWMQNVGAHVXSPE-UHFFFAOYSA-N ☒N

 ☒NcheckY (what is this?)  (verify)

Pyriprole (trade name Prac-tic) is for veterinary use on dogs against external parasites such as fleas and ticks.[1][2]

Pyriprole is a phenylpyrazole derivative similar to fipronil. Although recently introduced (in the 2000s) and still under patent protection it is a "classic" insecticide.[clarification needed] So far it is only approved in the EU and a few other countries for use on dogs. It is not approved for use on cats or livestock. It has not been introduced as an agricultural or hygiene pesticide.

Pyriprole applied as a spot-on is highly effective against fleas and several ticks species. Efficacy against fleas is comparable to that of other modern insecticidal active ingredients such as fipronil, imidaclopridorspinosad. As most flea spot-ons it controls existing flea and tick infestations in about 1 to 2 days, and provides about 4 weeks protection against re-infestations.

Mechanism of action

[edit]

Pyriprole is an insecticide and acaricide. It inhibits γ-aminobutyric acid (GABA)-gated chloride channels (GABAA receptors) resulting in uncontrolled hyperactivity of the central nervous system of fleas and ticks.

Parasites are killed through contact rather than by systemic exposure. Following topical administration pyriprole is rapidly distributed in the hair coat of dogs within one day after application. It can be found in the hair coat throughout the treatment interval. Insecticidal efficacy duration against new infestations with fleas persists for a minimum of four weeks. The substance can be used as part of a treatment strategy for the control of flea allergy dermatitis (FAD).

Warnings

[edit]

Do not use in dogs less than 8 weeks of age or with a body weight of less than 2 kg. Do not use in case of known hypersensitivity to phenylpyrazole class compounds or any of the excipients. Do not use on sick (e.g. systemic diseases, fever) or convalescent animals. This product is specifically developed for dogs. Do not use in cats, as this could lead to overdosing. Do not use on rabbits. The drug is for spot-on application only. Do not administer orally or via any other route.[3]

References

[edit]
  1. ^ Page SW (2008). "Antiparasitic Drugs". In Maddison JE, Page SW, Church DB (eds.). Small Animal Clinical Pharmacology (Second ed.). [Edinburgh]: Elsevier Health Sciences. pp. 198–260 (229). doi:10.1016/B978-070202858-8.50012-9. ISBN 978-0-7020-2858-8.
  • ^ Londershausen M, Hansen O (2008). "Ectoparasiticides – Antagonists and Modulators of Chloride Channels". In Mehlhorn H (ed.). Encyclopedia of Parasitology (3rd ed.). Berlin: Springer Rechtswissenschaft. p. 431. ISBN 978-3-540-48994-8.
  • ^ "Prac-tic (Pyriprole)". Novartis Animal Health Inc. 2013. Archived from the original on 2013-09-11. Retrieved 2013-09-14.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Pyriprole&oldid=1217278147"

    Categories: 
    Insecticides
    2-Pyridyl compounds
    Pyrazoles
    Nitriles
    Organofluorides
    Trifluoromethyl compounds
    Thioethers
    Chlorobenzene derivatives
    Synthetic insecticides
    3-Tolyl compounds
    4-Tolyl compounds
    Hidden categories: 
    Articles with short description
    Short description matches Wikidata
    Articles needing additional references from October 2013
    All articles needing additional references
    Articles with changed ChemSpider identifier
    Articles with changed InChI identifier
    Articles without EBI source
    Chemical pages without DrugBank identifier
    Articles without KEGG source
    Drugs with no legal status
    Drugboxes which contain changes to verified fields
    Drugboxes which contain changes to watched fields
    Wikipedia articles needing clarification from October 2013
     



    This page was last edited on 4 April 2024, at 21:40 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki