U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C7H5O2S.Na
Molecular Weight 176.168
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SODIUM THIOSALICYLATE

SMILES

[Na+].[O-]C(=O)C1=C(S)C=CC=C1

InChI

InChIKey=HBAIZOJDXAXWHS-UHFFFAOYSA-M
InChI=1S/C7H6O2S.Na/c8-7(9)5-3-1-2-4-6(5)10;/h1-4,10H,(H,8,9);/q;+1/p-1

HIDE SMILES / InChI
Thiosalicylic acid is an analgesic and anti-inflammatory agent. It is used (in form of sodium salt) to relieve symptoms of acute gout, painful musculoskeletal conditions, osteoarthritis and rheumatic fever. The drug exerts its action by inhibiting prostaglandin synthesis. Thiosalicylic acid usage is associated with the risk of contact dermatitis.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
REXOLATE

Approved Use

To relieve symptoms of acute gout, to relieve pain from musculoskeletal conditions, to relieve symptoms of osteoarthritis, to treat rheumatic fever.
Palliative
REXOLATE

Approved Use

To relieve symptoms of acute gout, to relieve pain from musculoskeletal conditions, to relieve symptoms of osteoarthritis, to treat rheumatic fever.
Palliative
REXOLATE

Approved Use

To relieve symptoms of acute gout, to relieve pain from musculoskeletal conditions, to relieve symptoms of osteoarthritis, to treat rheumatic fever.
Primary
REXOLATE

Approved Use

To relieve symptoms of acute gout, to relieve pain from musculoskeletal conditions, to relieve symptoms of osteoarthritis, to treat rheumatic fever.
PubMed

PubMed

TitleDatePubMed
Using model complexes to augment and advance metalloproteinase inhibitor design.
2004 May 17
Chelating sorbents based on silica gel and their application in atomic spectrometry.
2005 Mar
Determination of mercury complexation in coastal and estuarine waters using competitive ligand exchange method.
2005 Sep 1
In vitro-refolding of a single-chain Fv fragment in the presence of heteroaromatic thiols.
2008 Apr 30
Natural products as an inspiration in the diversity-oriented synthesis of bioactive compound libraries.
2008 Aug
[1,2-Bis(diphenyl-phosphino)ethane-κP,P'](2-carboxyl-atothio-phenolato-κO,S)nickel(II) methanol solvate.
2009 Jan 8
The Ras inhibitor farnesylthiosalicyclic acid (FTS) prevents nodule formation and development of preneoplastic foci of altered hepatocytes in rats.
2009 Jul
Expression of metallothionein mRNAs on mouse cerebellum microglia cells by thimerosal and its metabolites.
2009 Jun 30
Mercury exposure, nutritional deficiencies and metabolic disruptions may affect learning in children.
2009 Oct 27
2-[(2-Carboxy-phen-yl)sulfan-yl]acetic acid.
2009 Sep 5
Poly[(dimethyl-formamide)(μ(4)-2,2'-sulfanediyldibenzoato)nickel(II)].
2010 Mar 6
2-[(2-Carboxy-phen-yl)disulfan-yl]benzoic acid-4,4'-bipyridyl N,N'-dioxide (1/2).
2010 May 26
14-(1,3-Benzodioxol-5-yl)-7,14-dihydro-dibenzo[a,j]acridine.
2010 Nov 6
Patents

Sample Use Guides

Acute gout: initial dose is 100 mg every 3 to 4 hours for 2 days, then 100 mg daily. Painful musculoskeletal conditions: 50 to 100 mg daily or every other day. Osteoarthritis: 10 mg 3 times/week for several weeks then once a week, usually up to a total dosage of 2.5 g. Rheumatic fever: initial dose is 100 to 150 mg every 4 to 8 hours for 3 days, then 100 mg two times daily.
Route of Administration: Other
In Vitro Use Guide
Human platelets were incubated with thiosalicylic acid at 0.5 mM for 3 min in the presence of 1,2 and 1,3-glyceryl dinitrate. A concentration-dependent inhibition of platelet aggregation was observed.
Name Type Language
SODIUM THIOSALICYLATE
MART.   VANDF   WHO-DD  
Systematic Name English
SODIUM 2-SULFANYLBENZOATE
Systematic Name English
SODIUM THIOSALICYLATE [MART.]
Common Name English
Sodium thiosalicylate [WHO-DD]
Common Name English
SODIUM THIOSALICYLATE [VANDF]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
Code System Code Type Description
DRUG CENTRAL
4856
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
PRIMARY
EVMPD
SUB15331MIG
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
PRIMARY
FDA UNII
C2D9ITW04B
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
PRIMARY
NCI_THESAURUS
C87326
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
PRIMARY
RXCUI
91100
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
PRIMARY RxNorm
SMS_ID
100000078126
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
PRIMARY
CAS
134-23-6
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
PRIMARY
PUBCHEM
23681689
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID90928380
Created by admin on Fri Dec 15 15:19:20 GMT 2023 , Edited by admin on Fri Dec 15 15:19:20 GMT 2023
PRIMARY