Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H9AsN2O4 |
| Molecular Weight | 260.079 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)NC1=CC=C(C=C1)[As](O)(O)=O
InChI
InChIKey=WWXBHTZSYYGCSG-UHFFFAOYSA-N
InChI=1S/C7H9AsN2O4/c9-7(11)10-6-3-1-5(2-4-6)8(12,13)14/h1-4H,(H3,9,10,11)(H2,12,13,14)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Current treatment options for Dientamoeba fragilis infections. | 2012-12 |
|
| Virulence Of Entamoeba Histolytica According To The Strains In Korea: III. Amebicial Response Of Antiamoebic Agents On Several Strains Of Entamoeba Histolytica In Vitro. | 1969-12 |
|
| Trichomonas urethritis in males. | 1955-12 |
|
| Balantidial dysentery. | 1953-09 |
|
| Less commonly recognized clinical features of amebiasis. | 1952-04 |
|
| The mechanism of coprosterol formation in vivo: 2. Its inhibition by succinyl sulphathiazole and by carbarsone. | 1943 |
Patents
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|---|---|---|---|---|
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Preferred Name | English | ||
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Official Name | English | ||
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C277
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m3057
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8480
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121-59-5
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32868
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3065
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DTXSID4020246
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C76414
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100000081335
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204-484-6
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20206
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CARBARSONE
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384
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8PK70TXE1T
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C033007
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DB11382
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SUB06116MIG
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PRIMARY |
ACTIVE MOIETY