Acetarsol

Acetarsol
Names
Preferred IUPAC name
Acetarsone
Systematic IUPAC name
(3-Acetamido-4-hydroxyphenyl)arsonic acid[1]
Other names
3-Acetamido-4-hydroxyphenylarsonic acid
Identifiers
97-44-9 N
ChEMBL ChEMBL1330792 N
ChemSpider 1908 YesY
EC Number 202-582-3
Jmol 3D model Interactive image
Interactive image
KEGG D07110 YesY
MeSH Acetarsol
PubChem 1985
UNII 806529YU1N YesY
UN number 3465
Properties
C8H10AsNO5
Molar mass 275.0903 g mol−1
Pharmacology
A07AX02 (WHO) G01AB01 (WHO), P01CD02 (WHO), P51AD05 (WHO)
Hazards
GHS pictograms
GHS signal word Danger
H301, H331, H410
P261, P273, P301+310, P311, P501
T N
R-phrases R23/25, R50/53
S-phrases S20/21, S28, S45, S60, S61
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Acetarsol is an anti-infective.[2]

It was first discovered in 1921 at Pasteur Institute by Ernest Fourneau, and sold under the brand name Stovarsol (fourneau is the French word for stove).[3][4]

It has been given in suppositories.[5]

References

  1. "acetarsol - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information.
  2. 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.
  3. Éric Fouassier, Ces poisons qui guérissent, oct. 1996, p. 5.
  4. Traité de chimie organique, sous la direction de Victor Grignard, Paul Baud, vol. 22, Masson, 1959, p. 1127-1130.
  5. 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.
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