Weight | 260.081 g/mol |
---|---|
Formula | C7H9AsN2O4 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 4 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
Carbarsone (121-59-5)
4-ureidobenzenearsonic acid · Carbarson · Carbason
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- Carbarsone In the Treatment of Amebiasis. (JAMA, 1932)
- TOXICITY OF CARBARSONE: ACUTE FATTY DEGENERATION OF THE LIVER, EXFOLIATIVE DERMATITIS AND DEATH FOLLOWING ITS ADMINISTRATION (JAMA, 1936)
- CARBARSONE TOXICITY: A REVIEW OF THE LITERATURE AND REPORT OF 45 CASES (Annals of Internal Medicine, 1957)
- The mechanism of coprosterol formation in vivo: 2. Its inhibition by succinyl sulphathiazole and by carbarsone. (Biochemical Journal, 1943)
- p-AMINOBENZOIC ACID DETOXICATION OF CARBARSONE (p-CARBAMINO PHENYL ARSONIC ACID) AND CERTAIN OTHER PENTAVALENT PHENYL ARSONATES ADMINISTERED IN MASSIVE DOSES TO RATS. (Science, 1943)
- On the Effectiveness of Carbarsone as a Remedy for Amoebiasis. (American Journal of Tropical Medicine and Hygiene, 1938)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-ureidobenzenearsonic acid
- Carbarson
- Carbason
-
SMILESC1=CC(=CC=C1NC(=O)N)[As](=O)(O)O
-
InChIKeyWWXBHTZSYYGCSG-UHFFFAOYSA-N
- Pubchem - Carbarsone
- Wikipedia - carbarsone
Carbarsone is an organoarsenic compound used as an antiprotozoal drug for treatment of amebiasis and other infections. It was available for amebiasis in the United States as late as 1991. Thereafter, it remained available as a turkey feed additive for increasing weight gain and controlling histomoniasis (blackhead disease).
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