Details
Stereochemistry | ABSOLUTE |
Molecular Formula | 2C4H2O6.2K.2Sb.3H2O |
Molecular Weight | 667.873 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.O.[K+].[K+].[Sb+3].[Sb+3].[O-][C@H]([C@@H]([O-])C([O-])=O)C([O-])=O.[O-][C@H]([C@@H]([O-])C([O-])=O)C([O-])=O
InChI
InChIKey=WBTCZEPSIIFINA-MSFWTACDSA-J
InChI=1S/2C4H4O6.2K.3H2O.2Sb/c2*5-1(3(7)8)2(6)4(9)10;;;;;;;/h2*1-2H,(H,7,8)(H,9,10);;;3*1H2;;/q2*-2;2*+1;;;;2*+3/p-4/t2*1-,2-;;;;;;;/m11......./s1
Molecular Formula | HO |
Molecular Weight | 17.0073 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C4H4O6 |
Molecular Weight | 148.071 |
Charge | -2 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | K |
Molecular Weight | 39.0983 |
Charge | 1 |
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 |
---|---|---|
Current chemotherapy of schistosomiasis japonica in the Philippines. | 1976 Jun |
|
[Substantiation of maximum permissible levels of antimony trioxide and pentasulide in the atmospheric air of inhabitated places]. | 1989 Apr |
|
Antimony impairs nucleotide excision repair: XPA and XPE as potential molecular targets. | 2010 Jul 19 |
|
Investigation on the pharmacological profile of 2,6-diacetylpyridine bis(benzoylhydrazone) derivatives and their antimony(III) and bismuth(III) complexes. | 2012 Jul |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:39:06 GMT 2023
by
admin
on
Fri Dec 15 15:39:06 GMT 2023
|
Record UNII |
DL6OZ476V3
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C737
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
||
|
EPA PESTICIDE CODE |
6201
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
ANTIMONY POTASSIUM TARTRATE
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
28300-74-5
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
DL6OZ476V3
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
m1961
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | Merck Index | ||
|
100000077425
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
C76863
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
1428
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
2761
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
981
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | RxNorm | ||
|
SUB34747
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
73415808
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
DB15587
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
SUB127075
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
ALTERNATIVE | |||
|
SUB12916MIG
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
DL6OZ476V3
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY | |||
|
D000966
Created by
admin on Fri Dec 15 15:39:06 GMT 2023 , Edited by admin on Fri Dec 15 15:39:06 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ANHYDROUS->SOLVATE | |||
|
PARENT -> SALT/SOLVATE | |||
|
PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |