Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H10AsNO6S |
Molecular Weight | 311.144 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(NCS(O)=O)C=C(C=C1)[As](O)(O)=O
InChI
InChIKey=MSEAHRGTAGLWGR-UHFFFAOYSA-N
InChI=1S/C7H10AsNO6S/c10-7-2-1-5(8(11,12)13)3-6(7)9-4-16(14)15/h1-3,9-10H,4H2,(H,14,15)(H2,11,12,13)
Molecular Formula | C7H10AsNO6S |
Molecular Weight | 311.144 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Phenarsone sulfoxylate (Aldarsone), a pentavalent arsenical, is a condensation product of 3-amino-4 hydroxylphenylarsonic acid with sodium formaldehyde sulfoxylate. It is an antiamoebic agent. Aldarsone has a spirochetal power superior to that of tryparsamide. Aldarsone may be used in conjunction with artificial fever therapy and penicillin therapy to improve the results in symptomatic syphilis of the central nervous system (neurosyphilis).
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
The use of aldarsone in the treatment of neurosyphilis. | 1946 Jun |
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ALDARSONE IN NEURO-SYPHILIS. | 1946 Jun |
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Aldarsone and neurosyphilis. | 1947 Sep |
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Aldarsone therapy in the treatment of general paresis. | 1948 Aug |
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Aldarsone and bismuth combined in the treatment of neurosyphilis; report of 100 cases. | 1948 Jul |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:51:09 GMT 2023
by
admin
on
Fri Dec 15 18:51:09 GMT 2023
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Record UNII |
QEG0T4K3VZ
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Record Status |
Validated (UNII)
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Record Version |
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C184907
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100000082229
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |