Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Arprinocid

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Arprinocid
Ball-and-stick model of the arprinocid molecule
Clinical data
ATCvet code
Identifiers
  • 9-[(2-chloro-6-fluorophenyl)methyl]-6-purinamine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.054.362Edit this at Wikidata
Chemical and physical data
FormulaC12H9ClFN5
Molar mass277.69 g·mol−1
3D model (JSmol)
  • C1=CC(=C(C(=C1)Cl)CN2C=NC3=C2N=CN=C3N)F
  • 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) checkY
  • Key:NAPNOSFRRMHNBJ-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Arprinocid is acoccidiostat (or more likely a coccidiocide, i.e. a drug killingCoccidia parasites) used in veterinary medicine.[1]

Synthesis

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

References

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

Thisantiinfectivedrug article is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Arprinocid&oldid=1194226602"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp