Misplaced Pages

Arprinocid

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Chemical compound Pharmaceutical compound
Arprinocid
Ball-and-stick model of the arprinocid molecule
Clinical data
ATCvet code
Identifiers
IUPAC name
  • 9--6-purinamine
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.054.362 Edit this at Wikidata
Chemical and physical data
FormulaC12H9ClFN5
Molar mass277.69 gยทmol
3D model (JSmol)
SMILES
  • C1=CC(=C(C(=C1)Cl)CN2C=NC3=C2N=CN=C3N)F
InChI
  • InChI=1S/C12H9ClFN5/c13-8-2-1-3-9(14)7(8)4-19-6-18-10-11(15)16-5-17-12(10)19/h1-3,5-6H,4H2,(H2,15,16,17)
  • Key:NAPNOSFRRMHNBJ-UHFFFAOYSA-N
  (what is this?)  (verify)

Arprinocid is a coccidiostat (or more likely a coccidiocide, i.e. a drug killing Coccidia parasites) used in veterinary medicine.

Synthesis

Arprinocid synthesis: Merck & Co. R. J. Tull, G. D. Hartman, and L. M. Weinstock, U.S. patent 4,098,787 (1978).

References

  1. McQuistion TE, McDougald LR (October 1981). "Anticoccidial activity of arprinocid and halofuginone". Veterinary Parasitology. 9 (1): 27โ€“33. doi:10.1016/0304-4017(81)90004-2. PMID 7201182.
Stub icon

This antiinfective drug article is a stub. You can help Misplaced Pages by expanding it.

Categories: