Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | 3I.Sb |
| Molecular Weight | 502.473 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Sb+3].[I-].[I-].[I-]
InChI
InChIKey=KWQLUUQBTAXYCB-UHFFFAOYSA-K
InChI=1S/3HI.Sb/h3*1H;/q;;;+3/p-3
| Molecular Formula | HI |
| Molecular Weight | 127.91241 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | Sb |
| Molecular Weight | 121.76 |
| Charge | 3 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.whocc.no/atcvet/atcvet_index/?code=QR05CA07https://www.ncbi.nlm.nih.gov/pubmed/5295139 | https://www.ncbi.nlm.nih.gov/pubmed/14851220 | https://www.ncbi.nlm.nih.gov/pubmed/8898332Curator's Comment: description was created based on several sources, including https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7ef48d40-6d63-440b-a73c-46d89f425936
Sources: https://www.whocc.no/atcvet/atcvet_index/?code=QR05CA07https://www.ncbi.nlm.nih.gov/pubmed/5295139 | https://www.ncbi.nlm.nih.gov/pubmed/14851220 | https://www.ncbi.nlm.nih.gov/pubmed/8898332
Curator's Comment: description was created based on several sources, including https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7ef48d40-6d63-440b-a73c-46d89f425936
Stibophen (Fuadin), an organic trivalent antimony compound, has been used for many years in the treatment of schistosomiasis. Stibophen is used as treatment of schistosomiasis by intramuscular injection. Stibophen is known to act by selectively inhibiting worm PFK.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Investigation on the pharmacological profile of 2,6-diacetylpyridine bis(benzoylhydrazone) derivatives and their antimony(III) and bismuth(III) complexes. | 2012-07 |
|
| Antimony impairs nucleotide excision repair: XPA and XPE as potential molecular targets. | 2010-07-19 |
|
| Purification, kinetics and inhibition by antimonials of recombinant phosphofructokinase from Schistosoma mansoni. | 1996-10-30 |
|
| [Substantiation of maximum permissible levels of antimony trioxide and pentasulide in the atmospheric air of inhabitated places]. | 1989-04 |
|
| Current chemotherapy of schistosomiasis japonica in the Philippines. | 1976-06 |
|
| Laboratory studies on the joint effects of certain tris (p-aminophenyl) carbonium salts and antimonials as antischistosomal drugs. | 1965 |
|
| Evaluation of fuadin therapy in schistosomiasis japonica. | 1951-04 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:16:40 GMT 2025
by
admin
on
Mon Mar 31 18:16:40 GMT 2025
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| Record UNII |
52ZE5Y9Y82
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| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C579
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C87427
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232-205-8
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ANTIMONY TRIIODIDE
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437
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52ZE5Y9Y82
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300000052598
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DTXSID1064875
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24630
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7790-44-5
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52ZE5Y9Y82
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1423913
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m1968
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PRIMARY | Merck Index |
| Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |