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Details

Stereochemistry RACEMIC
Molecular Formula C3H8O3S3
Molecular Weight 188.289
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3-DIMERCAPTO-1-PROPANESULFONIC ACID

SMILES

OS(=O)(=O)CC(S)CS

InChI

InChIKey=JLVSRWOIZZXQAD-UHFFFAOYSA-N
InChI=1S/C3H8O3S3/c4-9(5,6)2-3(8)1-7/h3,7-8H,1-2H2,(H,4,5,6)

HIDE SMILES / InChI

Molecular Formula C3H8O3S3
Molecular Weight 188.289
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Unithiol was developed in the Soviet Union in the late 1950s. It only became more widely used in America and Western Europe since the mid-1970s, and particularly since the late 1970s when the Heyl Company in Germany began production. It remained the mainstay of chelation treatment of arsenic and mercury intoxication for more than half a century. Unithiol has been used in the management of acute and chronic poisoning with a number of different metals and metalloids, and is particularly useful for arsenic, bismuth and mercury. Unithiol can be given parenterally or orally depending on the clinical situation and severity of poisoning. Its action mechanism is close that of complexones. Active sulfhydryl groups enter into reactions with thiol poisons present in blood and tissues, form not toxic complex with them eliminated with urine. The poisons fixation results in the body enzyme systems changed under the poisons effect functions restoration. It is efficient as an antidote in case of intoxications by arsenic and heavy metals salts.

CNS Activity

Curator's Comment: DMPS can cross the blood–brain barrier of mice, but not that of humans, limiting its use to extracting heavy metals from parts of the body other than the central nervous system.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
DIMAVAL

Approved Use

Dimaval is used for cases of acute mercury poisoning (metallic, vapour, inorganic or organic compounds), if application by mouth or treatment by means of a gastric aspiration tube are not possible.
PubMed

PubMed

TitleDatePubMed
[Oxidative stress of acute paraquat poisoned rats and sodium dimercaptopropane sulfonate intervention].
2009 Aug
[Expression of thrombomodulin, endothelial protein C receptor in lung tissue of acute paraquat poisoned rats and intervention of sodium dimercaptopropane sulfonate].
2009 Aug
Effects of co-administration of dietary sodium arsenate and 2,3-dimercaptopropane-1-sulfonic acid (DMPS) on the rat bladder epithelium.
2012 Sep 28
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: can also be used orally https://www.ncbi.nlm.nih.gov/pubmed/12711426
For managing acute and chronic intoxications by arsenic and mercury compounds utnithiol is injected intramuscular or subcutaneous (5 – 10 ml of 5% solution). The treatment should be started as early as possible. In case of intoxications by arsenic compounds injections are every 6 – 8 hours the first day, 2 – 3 injections every 8 – 12 hours the second day, 1 – 2 injections the subsequent days. Children are made intramuscular injections in the doses 1 ml of 5% solution for each 10 kg of the body mass every 6 hours the first day; then 1 – 3 injections a day. In case of intoxications by mercury salts the preparation is injected for not less than 6 days. In case of intoxications by cardiac glicosides it is injected intramuscular or subcutaneous in the dose 5 or 10 ml of the unithiol 5% solution during the first 2 days. Injections are made 3 – 4 times a day. Then it is injected 1 – 2 times a day until the cardiotoxic action stops. In case of hepatocerebral degeneration 5 – 10 ml of the unithiol solution is prescribed for daily or in a day intramuscular injections, the course being 25 – 30 injections with an interval between the courses – 3 – 4 months. In case of diabetic polyneuropathy 5 ml of 5% solution is injected for 10 days. In case of chronic alcoholism the preparation is introduced intramuscular in dose 3 – 5 ml of 5% solution 2 – 3 times a week. For arresting the alcoholic delirium attacks 4 – 5ml of 5% solution is injected intramuscular. 1 ml of the preparation contains 50 mg of unithiol.
Route of Administration: Other
When HepG2 cells were co-treated with As3+ (25 uM) and DMPS (Unithiol) (0.02, 0.2, 1.0, or 2.0 mM), cellular arsenic was decreased with the increasing of DMPS concentration from 0.02 mM to 2.0 mM. DMPS at high concentration (>1.0 mM) dramatically decreased the accumulation of arsenic in HepG2 cells. The cellular arsenic was decreased from 5.72% to 0.13% when the cells were treated with 2.0 mM DMPS.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:09:28 GMT 2023
Edited
by admin
on Fri Dec 15 15:09:28 GMT 2023
Record UNII
086L82361J
Record Status Validated (UNII)
Record Version
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Name Type Language
2,3-DIMERCAPTO-1-PROPANESULFONIC ACID
MI  
Systematic Name English
2,3-DIMERCAPTO-1-PROPANE SULFONATE
Common Name English
(±)-2,3-DIMERCAPTO-1-PROPANESULFONIC ACID
Systematic Name English
DMPS
Common Name English
DIMERCAPTOPROPANE SULFONIC ACID
Systematic Name English
1-PROPANESULFONIC ACID, 2,3-DIMERCAPTO-
Common Name English
2,3-DIMERCAPTO-1-PROPANESULFONIC ACID [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C62357
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID5048344
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
FDA UNII
086L82361J
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
DAILYMED
086L82361J
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
RXCUI
1546352
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY RxNorm
WIKIPEDIA
2,3-Dimercapto-1-propanesulfonic acid
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
CHEBI
888
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
CAS
74-61-3
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
EVMPD
SUB121460
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
SMS_ID
100000144630
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
MERCK INDEX
m4502
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY Merck Index
PUBCHEM
6321
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
NCI_THESAURUS
C87416
Created by admin on Fri Dec 15 15:09:28 GMT 2023 , Edited by admin on Fri Dec 15 15:09:28 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
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ACTIVE MOIETY