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Contents

   



(Top)
 


1 Medical uses  





2 Mechanism of action  





3 Chemistry and pharmacokinetics  





4 Toxicity  





5 References  














Acetarsol






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From Wikipedia, the free encyclopedia
 


Acetarsol
Kekulé, skeletal formula of acetarsol
Names
Preferred IUPAC name

(3-Acetamido-4-hydroxyphenyl)arsonic acid

Other names

Acetarsone

Identifiers

CAS Number

3D model (JSmol)

  • Interactive image
  • ChEBI
    ChEMBL
    ChemSpider
    DrugBank
    ECHA InfoCard 100.002.349 Edit this at Wikidata
    EC Number
    • 202-582-3
    KEGG
    MeSH Acetarsol

    PubChem CID

    UNII
    UN number 3465

    CompTox Dashboard (EPA)

    • InChI=1S/C8H10AsNO5/c1-5(11)10-7-4-6(9(13,14)15)2-3-8(7)12/h2-4,12H,1H3,(H,10,11)(H2,13,14,15) checkY

      Key: ODFJOVXVLFUVNQ-UHFFFAOYSA-N checkY

    • InChI=1/C8H10AsNO5/c1-5(11)10-7-4-6(9(13,14)15)2-3-8(7)12/h2-4,12H,1H3,(H,10,11)(H2,13,14,15)

      Key: ODFJOVXVLFUVNQ-UHFFFAOYAX

    • CC(=O)Nc1cc(ccc1O)[As](O)(O)=O

    • CC(=O)NC1=CC(=CC=C1O)[As](O)(O)=O

    Properties

    Chemical formula

    C8H10AsNO5
    Molar mass 275.0903 g mol−1
    Pharmacology

    ATC code

    A07AX02 (WHO) G01AB01 (WHO), P01CD02 (WHO), P51AD05 (WHO)
    Hazards
    GHS labelling:

    Pictograms

    GHS06: Toxic GHS09: Environmental hazard

    Signal word

    Danger

    Hazard statements

    H301, H331, H410

    Precautionary statements

    P261, P273, P301+P310, P311, P501

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Acetarsol (oracetarsone[1]) is an anti-infective drug.[2]

    It was first discovered in 1921 at Pasteur InstitutebyErnest Fourneau,[3] and sold under the brand name Stovarsol.[4][5] It has been given in the form of suppositories.[6]

    Acetarsol can be used to make arsthinol.[citation needed]

    It has been cancelled and withdrawn from the market since August 12th, 1997.[3]

    Medical uses[edit]

    Acetarsol has been used for the treatment of diseases such as syphilis, amoebiasis, yaws, trypanosomiasisiasis and malaria. Acetarsol was used for the treatment of Trichomonas Vaginalis and Candida Albicans. In the oral form, acetarsol can be used for the treatment of intestinal amoebiasis. As a suppository, acetarsol was researched to be used for the treatment of proctitis.[3]

    Mechanism of action[edit]

    Although the mechanism of action is not fully known, acetarsol may bind to protein-containing sulfhydryl groups located in the parasite, which then creates lethal As-S bonds, which then kills the parasite. [3]

    Chemistry and pharmacokinetics[edit]

    Acetarsol has the molecular formula N-acetyl-4-hydroxy-m-arsinillic acid, and it is a pentavalent arsenical compound with antiprotozoal and anthelmintic properties. The arsenic found in acetarsol is excreted mainly in urine. The level of arsenic after acetarsol administration reaches close to the toxic range in urine.[3] Some reports indicate a remission of arsenic which can be physiologically dangerous. [3]

    Toxicity[edit]

    Some reports indicate that acetarsol can produce effects in the eyes such as optic neuritis and optic atrophy.[7]

    References[edit]

    1. ^ "FDA Substance Registration System: Acetarsol". Archived from the original on 8 January 2021. Retrieved 6 May 2021.
  • ^ Chen MY, Smith NA, Fox EF, Bingham JS, Barlow D (April 1999). "Acetarsol pessaries in the treatment of metronidazole resistant Trichomonas vaginalis". Int J STD AIDS. 10 (4): 277–80. doi:10.1258/0956462991913943. PMID 12035784. S2CID 27353282.
  • ^ a b c d e f PubChem. "Acetarsol". pubchem.ncbi.nlm.nih.gov. Retrieved 2021-03-31.
  • ^ "Éric Fouassier, Ces poisons qui guérissent, oct. 1996, p. 5" (PDF). Archived from the original (PDF) on 2011-10-05. Retrieved 2010-04-01.
  • ^ Traité de chimie organique, sous la direction de Victor Grignard, Paul Baud, vol. 22, Masson, 1959, p. 1127-1130.
  • ^ Gionchetti P, Rizzello F, Morselli C, Campieri M (October 2004). "Review article: problematic proctitis and distal colitis". Aliment. Pharmacol. Ther. 20 (Suppl 4): 93–6. doi:10.1111/j.1365-2036.2004.02049.x. PMID 15352902. S2CID 72699260.
  • ^ PubChem. "Acetarsol". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-01-16.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Acetarsol&oldid=1230043076"

    Categories: 
    Antiprotozoal agents
    Acetanilides
    Arsonic acids
    Phenols
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