Details
Stereochemistry | MIXED |
Molecular Formula | C13H11AsN6O4S2.2K |
Molecular Weight | 532.512 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 0 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[K+].[K+].NC1=NC(NC2=CC=C(C=C2)[As]3SC(C(S3)C([O-])=O)C([O-])=O)=NC(N)=N1
InChI
InChIKey=PHCMFHVCRUCADN-UHFFFAOYSA-L
InChI=1S/C13H13AsN6O4S2.2K/c15-11-18-12(16)20-13(19-11)17-6-3-1-5(2-4-6)14-25-7(9(21)22)8(26-14)10(23)24;;/h1-4,7-8H,(H,21,22)(H,23,24)(H5,15,16,17,18,19,20);;/q;2*+1/p-2
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
[POTASSIUM MELARSONYL IN THE TREATMENT OF HUMAN ONCHOCERCIASIS. PRELIMINARY NOTE. FINDINGS AFTER 10 MONTHS OF OBSERVATION]. | 1964 May-Jul |
|
The effects of drugs on Onchocerca volvulus. 4. Trials of melarsonyl potassium. | 1970 |
|
Synthesis and in vitro anthelmintic properties of some new dithiaarsanes. | 1999 Nov |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/5309509
The effects of the arsenical drug melarsonyl potassium on Onchocerca volvulus were investigated in patients in Cameroon infected with the Cameroon forest and Sudan savanna strains of the parasite. Two intramuscular dosage schedules were tested: the first comprised 4 consecutive daily doses of 200 mg repeated once after a 10-14 day interval, i.e., 2 (4x200 mg). The second was a single dose schedule at 7.1 mg/kg-10 mg/kg, with a maximum of 500 mg.
Route of Administration:
Intramuscular
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10604048
On the M. dessetae model after a 24 h incubation period potassium melarsonyl exhibited an EC50 of 45.6 uM.
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Code | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
SUB08720MIG
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
PRIMARY | |||
|
C166459
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
PRIMARY | |||
|
100000081465
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
PRIMARY | |||
|
236-405-6
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
PRIMARY | |||
|
1484SU81EQ
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
PRIMARY | |||
|
DTXSID70928181
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
PRIMARY | |||
|
1256
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
PRIMARY | |||
|
16173-18-5
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
NON-SPECIFIC STOICHIOMETRY | |||
|
13355-00-5
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
PRIMARY | |||
|
25907
Created by
admin on Sat Dec 16 16:55:14 GMT 2023 , Edited by admin on Sat Dec 16 16:55:14 GMT 2023
|
PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD