Misplaced Pages

Arprinocid: Difference between revisions

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.
Browse history interactively← Previous editContent deleted Content addedVisualWikitext
Revision as of 14:54, 24 October 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{drugbox}} (changes to verified fields - added verified revid - updated 'ChEMBL_Ref', 'ChEBI_Ref', 'CAS_number_Ref') per Chem/Drugbox validation (report errors or [[user talk:C...← Previous edit Latest revision as of 22:24, 7 January 2024 edit undoMichael7604 (talk | contribs)Extended confirmed users8,895 edits recategorized from Chlorobenzenes to Chlorobenzene derivatives 
(17 intermediate revisions by 15 users not shown)
Line 1: Line 1:
{{Short description|Chemical compound}}
{{Drugbox {{Drugbox
| Verifiedfields = changed | Verifiedfields = changed
Line 4: Line 5:
| IUPAC_name = 9--6-purinamine | IUPAC_name = 9--6-purinamine
| image = arprinocid.png | image = arprinocid.png
| image2 = Arprinocid molecule ball.png
| alt2 = Ball-and-stick model of the arprinocid molecule
| width2 = 240


<!--Clinical data--> <!--Clinical data-->
| tradename = | tradename =
| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> | pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X -->
| pregnancy_US = <!-- A / B / C / D / X --> | pregnancy_US = <!-- A / B / C / D / X -->
| pregnancy_category = | pregnancy_category =
| legal_AU = <!-- S2, S3, S4, S5, S6, S7, S8, S9 or Unscheduled--> | legal_AU = <!-- S2, S3, S4, S5, S6, S7, S8, S9 or Unscheduled-->
| legal_CA = <!-- Schedule I, II, III, IV, V, VI, VII, VIII --> | legal_CA = <!-- Schedule I, II, III, IV, V, VI, VII, VIII -->
| legal_UK = <!-- GSL, P, POM, CD, or Class A, B, C --> | legal_UK = <!-- GSL, P, POM, CD, or Class A, B, C -->
| legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V --> | legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V -->
| legal_status = | legal_status =
| routes_of_administration = | routes_of_administration =


<!--Pharmacokinetic data--> <!--Pharmacokinetic data-->
| bioavailability = | bioavailability =
| protein_bound = | protein_bound =
| metabolism = | metabolism =
| elimination_half-life = | elimination_half-life =
| excretion = | excretion =


<!--Identifiers--> <!--Identifiers-->
Line 34: Line 38:
| PubChem = 41574 | PubChem = 41574
| DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = | DrugBank =
| UNII_Ref = {{fdacite|correct|FDA}} | UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 6A0XTA8ZUH | UNII = 6A0XTA8ZUH
Line 41: Line 45:


<!--Chemical data--> <!--Chemical data-->
| C=12 | H=9 | Cl=1 | F=1 | N=5 | C=12 | H=9 | Cl=1 | F=1 | N=5
| molecular_weight = 277.68 g/mol
| smiles = C1=CC(=C(C(=C1)Cl)CN2C=NC3=C2N=CN=C3N)F | smiles = C1=CC(=C(C(=C1)Cl)CN2C=NC3=C2N=CN=C3N)F
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 37936 | ChemSpiderID = 37936
| InChI = 1/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)
| InChIKey = NAPNOSFRRMHNBJ-UHFFFAOYAV
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 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) | StdInChI = 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)
Line 54: Line 55:
}} }}


'''Arprinocid''' is a ] (or more likely a coccidiocide, i.e. a drug killing '']'' parasites) used in veterinary medicine.<ref>{{cite journal | vauthors = McQuistion TE, McDougald LR | title = Anticoccidial activity of arprinocid and halofuginone | journal = Veterinary Parasitology | volume = 9 | issue = 1 | pages = 27–33 | date = October 1981 | pmid = 7201182 | doi = 10.1016/0304-4017(81)90004-2 }}</ref>
'''Arprinocid''' is a ] used in veterinary medicine.
==Synthesis==

] R. J. Tull, G. D. Hartman, and L. M. Weinstock, {{US Patent|4,098,787}} (1978).]]
== References ==
{{reflist}}


] ]
] ]
] ]
] ]



{{antiinfective-drug-stub}} {{antiinfective-drug-stub}}

Latest revision as of 22:24, 7 January 2024

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 g·mol
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): 27–33. 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: