Acetarsol

Acetarsol
	Kekulé, skeletal formula of acetarsol
Names
	Preferred IUPAC name Acetarsone[citation needed]
	Systematic IUPAC name (3-Acetamido-4-hydroxyphenyl)arsonic acid
	Other names 3-Acetamido-4-hydroxyphenylarsonic acid[citation needed]
Identifiers
CAS Number	97-44-9 ;
3D model (JSmol)	Interactive image; Interactive image;
ChEMBL	ChEMBL1330792 ;
ChemSpider	1908 ;
ECHA InfoCard	Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value).
KEGG	D07110 ;
MeSH	Acetarsol
PubChem CID	1985;
UNII	806529YU1N ;
	InChI 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) Key: ODFJOVXVLFUVNQ-UHFFFAOYSA-N ; 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;
	SMILES CC(=O)Nc1cc(ccc1O)[As](O)(O)=O; CC(=O)NC1=CC(=CC=C1O)[As](O)(O)=O;
Properties
Chemical formula	C; 8AsNH; 10O; 5
Molar mass	275.0903 g mol−1
Hazards
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Template:Chembox ECNumber Template:Chembox E number Template:Chembox UNNumber Template:Chembox GHSPictograms Template:Chembox GHSSignalWord Template:Chembox HPhrases Template:Chembox PPhrases

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

↑ "acetarsol - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information.
↑ 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.

Template:Antidiarrheals, intestinal anti-inflammatory/anti-infective agents Template:Agents against leishmaniasis and trypanosomiasis

Template:Gastrointestinal-drug-stub Template:Antiinfective-drug-stub Template:Genito-urinary-drug-stub

[1] "acetarsol - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information.

[pmid12035784-2] 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.

[pmid15352902-5] 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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Names
Kekulé, skeletal formula of acetarsol
Preferred IUPAC name Acetarsone^{[citation needed]}
Systematic IUPAC name (3-Acetamido-4-hydroxyphenyl)arsonic acid^[1]
Other names 3-Acetamido-4-hydroxyphenylarsonic acid^{[citation needed]}
Identifiers
CAS Number	97-44-9^N
3D model (JSmol)	Interactive image Interactive image
ChEMBL	ChEMBL1330792^N
ChemSpider	1908^Y
ECHA InfoCard	Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value).
KEGG	D07110^Y
MeSH	Acetarsol
PubChem CID	1985
UNII	806529YU1N^Y
InChI 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)^Y Key: ODFJOVXVLFUVNQ-UHFFFAOYSA-N^Y 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
SMILES CC(=O)Nc1cc(ccc1O)[As](O)(O)=O CC(=O)NC1=CC(=CC=C1O)[As](O)(O)=O
Properties
Chemical formula	C ₈AsNH ₁₀O ₅
Molar mass	275.0903 g mol⁻¹
Hazards
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

Acetarsol

References

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