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)
Molecular Formula | C7H9AsN2O4 |
Molecular Weight | 260.079 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
The mechanism of coprosterol formation in vivo: 2. Its inhibition by succinyl sulphathiazole and by carbarsone. | 1943 |
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Less commonly recognized clinical features of amebiasis. | 1952 Apr |
|
Balantidial dysentery. | 1953 Sep |
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Trichomonas urethritis in males. | 1955 Dec |
|
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 Dec |
|
Current treatment options for Dientamoeba fragilis infections. | 2012 Dec |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:02:34 GMT 2023
by
admin
on
Fri Dec 15 15:02:34 GMT 2023
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Record UNII |
8PK70TXE1T
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C277
Created by
admin on Fri Dec 15 15:02:34 GMT 2023 , Edited by admin on Fri Dec 15 15:02:34 GMT 2023
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Code System | Code | Type | Description | ||
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m3057
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PRIMARY | Merck Index | ||
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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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PRIMARY | |||
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C76414
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PRIMARY | |||
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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
Created by
admin on Fri Dec 15 15:02:34 GMT 2023 , Edited by admin on Fri Dec 15 15:02:34 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |