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Details

Stereochemistry ACHIRAL
Molecular Formula C7H4I2O3
Molecular Weight 389.9138
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,5-DIIODOSALICYLIC ACID

SMILES

OC(=O)C1=CC(I)=CC(I)=C1O

InChI

InChIKey=DHZVWQPHNWDCFS-UHFFFAOYSA-N
InChI=1S/C7H4I2O3/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2,10H,(H,11,12)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Benzene exposure near the U.S. permissible limit is associated with sperm aneuploidy.
2010-06
Transthyretin-related familial amyloidotic polyneuropathy-Progress in Kumamoto, Japan (1967-2010)-.
2010
Modeling kinetics of subcellular disposition of chemicals.
2009-05
Differential nuclear scaffold/matrix attachment marks expressed genes.
2009-02-15
DNA flow cytometry of human spermatozoa: consistent stoichiometric staining of sperm DNA using a novel decondensation protocol.
2008-10
Iodination of salicylic acid improves its binding to transthyretin.
2008-03
A salicylic acid-based analogue discovered from virtual screening as a potent inhibitor of human 20alpha-hydroxysteroid dehydrogenase.
2007-11
Relationship between nuclear chromatin decondensation (NCD) in vitro and other sperm parameters and their predictive value on fertilization rate in IVF program.
2005-08
Interaction of bilirubin with native and protein-depleted human erythrocyte membranes.
2003-04
Patents
Name Type Language
3,5-DIIODOSALICYLIC ACID
MI  
Systematic Name English
NSC-6303
Preferred Name English
3,5-DIIODOSALICYLIC ACID [MI]
Common Name English
CLOSANTEL SODIUM DIHYDRATE IMPURITY A [EP IMPURITY]
Common Name English
2-HYDROXY-3,5-DIIODOBENZOIC ACID
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
205-124-0
Created by admin on Mon Mar 31 17:54:00 GMT 2025 , Edited by admin on Mon Mar 31 17:54:00 GMT 2025
PRIMARY
MERCK INDEX
m4478
Created by admin on Mon Mar 31 17:54:00 GMT 2025 , Edited by admin on Mon Mar 31 17:54:00 GMT 2025
PRIMARY Merck Index
DRUG BANK
DB04674
Created by admin on Mon Mar 31 17:54:00 GMT 2025 , Edited by admin on Mon Mar 31 17:54:00 GMT 2025
PRIMARY
FDA UNII
1496OH15B6
Created by admin on Mon Mar 31 17:54:00 GMT 2025 , Edited by admin on Mon Mar 31 17:54:00 GMT 2025
PRIMARY
PUBCHEM
8631
Created by admin on Mon Mar 31 17:54:00 GMT 2025 , Edited by admin on Mon Mar 31 17:54:00 GMT 2025
PRIMARY
CAS
133-91-5
Created by admin on Mon Mar 31 17:54:00 GMT 2025 , Edited by admin on Mon Mar 31 17:54:00 GMT 2025
PRIMARY
EPA CompTox
DTXSID3059636
Created by admin on Mon Mar 31 17:54:00 GMT 2025 , Edited by admin on Mon Mar 31 17:54:00 GMT 2025
PRIMARY
NSC
6303
Created by admin on Mon Mar 31 17:54:00 GMT 2025 , Edited by admin on Mon Mar 31 17:54:00 GMT 2025
PRIMARY