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Details

Stereochemistry ACHIRAL
Molecular Formula C2H3AsO5.2Na.H2O
Molecular Weight 245.9586
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DISODIUM ARSONOACETATE MONOHYDRATE

SMILES

O.[Na+].[Na+].O[As]([O-])(=O)CC([O-])=O

InChI

InChIKey=RJTDUAJFVQDGBM-UHFFFAOYSA-L
InChI=1S/C2H5AsO5.2Na.H2O/c4-2(5)1-3(6,7)8;;;/h1H2,(H,4,5)(H2,6,7,8);;;1H2/q;2*+1;/p-2

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including: Wilson, P.S. (2009) "Rediscovering Arsenoacetic Acid", p.9 Retrieved from http://researchcommons.waikato.ac.nz/bitstream/handle/10289/2778/thesis.pdf?sequence=1

Disodiurn salt of Arsonoacetic acid has been used in veterinary to treat anaplasmosis (babesiasis); as general stimulant in nervous disease; for eclampsia of bitches, and with adjuncts in chronic eczema and follicular mange. Arsonoacetic acid has not featured much in human medicine, a Chinese patent however, was filed in 2003 for arsonoacetic acid and its methyl or ethyl derivatives as chemotherapeutic drugs again liver cancer.

Originator

Sources: DOI: 10.1002/cber.191004301156

Approval Year

PubMed

PubMed

TitleDatePubMed
Tumor cell-specific prodrugs using arsonic acid-presenting iron oxide nanoparticles with high sensitivity.
2012-08-01
Arsonic acid-presenting superparamagnetic iron oxide for pH-responsive aggregation under slightly acidic conditions.
2011-04-01
The construction of a whole-cell biosensor for phosphonoacetate, based on the LysR-like transcriptional regulator PhnR from Pseudomonas fluorescens 23F.
2009-03
Carbon-arsenic bond cleavage by a newly isolated gram-negative bacterium, strain ASV2.
1995-03
The mechanism of pyrophosphorolysis of RNA by RNA polymerase. Endowment of RNA polymerase with artificial exonuclease activity.
1984-12-01
Mode of action of phosphonoformate as an anti-herpes simplex virus agent.
1981-01-29
Patents

Patents

Sample Use Guides

Horses, Cattle 10 ml Sheep, Goats 2-5 ml Big dogs 1.2 ml Dogs, Cats 0.2-0.5 ml Each ml contains 50 mg of disodium arsonoacetate.
Route of Administration: Other
In Vitro Use Guide
Unknown
Name Type Language
ARSONOACETIC ACID SODIUM SALT MONOHYDRATE
MI  
Preferred Name English
DISODIUM ARSONOACETATE MONOHYDRATE
Systematic Name English
ACETIC ACID, 2-ARSONO-, SODIUM SALT, HYDRATE (1:2:1)
Common Name English
ARICYL
Brand Name English
ARSONOACETIC ACID SODIUM SALT MONOHYDRATE [MI]
Common Name English
ARSONOACETIC ACID DISODIUM SALT MONOHYDRATE
Common Name English
DISODIUM ACETARSENATE MONOHYDRATE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID40208922
Created by admin on Mon Mar 31 21:43:31 GMT 2025 , Edited by admin on Mon Mar 31 21:43:31 GMT 2025
PRIMARY
MERCK INDEX
m2070
Created by admin on Mon Mar 31 21:43:31 GMT 2025 , Edited by admin on Mon Mar 31 21:43:31 GMT 2025
PRIMARY Merck Index
FDA UNII
NI6S09757V
Created by admin on Mon Mar 31 21:43:31 GMT 2025 , Edited by admin on Mon Mar 31 21:43:31 GMT 2025
PRIMARY
CAS
6018-31-1
Created by admin on Mon Mar 31 21:43:31 GMT 2025 , Edited by admin on Mon Mar 31 21:43:31 GMT 2025
PRIMARY
PUBCHEM
45048892
Created by admin on Mon Mar 31 21:43:31 GMT 2025 , Edited by admin on Mon Mar 31 21:43:31 GMT 2025
PRIMARY