Details
Stereochemistry | RACEMIC |
Molecular Formula | C11H14AsNO3S2 |
Molecular Weight | 347.285 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NC1=C(O)C=CC(=C1)[As]2SCC(CO)S2
InChI
InChIKey=MRUDSZSRLQAPOG-UHFFFAOYSA-N
InChI=1S/C11H14AsNO3S2/c1-7(15)13-10-4-8(2-3-11(10)16)12-17-6-9(5-14)18-12/h2-4,9,14,16H,5-6H2,1H3,(H,13,15)
Molecular Formula | C11H14AsNO3S2 |
Molecular Weight | 347.285 |
Charge | 0 |
Count |
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Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
The treatment of amebiasis with arsthinol (N.N.R) (balarsen). | 1954 Jun |
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Arsthinol (balarsen), a new trivalent arsenical for the treatment of intestinal amebiasis and other intestinal protozoa. | 1954 Mar |
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Intestinal amebiasis; incidence, symptoms, and treatment with arsthinol (balarsen). | 1956 Feb 4 |
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The antitumor effects of an arsthinol-cyclodextrin complex in a heterotopic mouse model of glioma. | 2013 Nov |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:14:54 GMT 2023
by
admin
on
Fri Dec 15 15:14:54 GMT 2023
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Record UNII |
QNT09A162Y
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Record Status |
Validated (UNII)
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Record Version |
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Official Name | English | ||
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Common Name | English | ||
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Classification Tree | Code System | Code | ||
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WHO-ATC |
P01AR01
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WHO-VATC |
QP51AD01
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3007
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QNT09A162Y
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DTXSID40861753
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DB08928
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8414
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ARSTHINOL
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240
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SUB05572MIG
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100000086623
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C76411
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C546471
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119-96-0
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m2072
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PRIMARY | Merck Index | ||
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204-361-7
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |