Acetarsol
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| Names | |
|---|---|
| Preferred IUPAC name
(3-Acetamido-4-hydroxyphenyl)arsonic acid | |
| Other names
3-Acetamido-4-hydroxyphenylarsonic acid[citation needed]
Acetarsol | |
| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.349 |
| EC Number |
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| KEGG | |
| MeSH | Acetarsol |
PubChem CID
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| UNII | |
| UN number | 3465 |
CompTox Dashboard (EPA)
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| Properties | |
| C8H10AsNO5 | |
| Molar mass | 275.0903 g mol−1 |
| Pharmacology | |
| A07AX02 (WHO) G01AB01 (WHO), P01CD02 (WHO), P51AD05 (WHO) | |
| Hazards | |
| GHS labelling: | |
 
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| Danger | |
| H301, H331, H410 | |
| 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).
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Acetarsol is an anti-infective.[1]
It was first discovered in 1921 at Pasteur Institute by Ernest Fourneau, and sold under the brand name Stovarsol[2][3]
It has been given in suppositories.[4]
Acetarsol can be used to make Arsthinol, & presumably Acetarsone also.
References
- ^ 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.
- ^ Éric Fouassier, Ces poisons qui guérissent, oct. 1996, p. 5.
- ^ 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.
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