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Details

Stereochemistry ACHIRAL
Molecular Formula C21H15O2.Na
Molecular Weight 322.3324
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MONOSODIUM SQUOXINATE

SMILES

[Na+].OC1=CC=C2C=CC=CC2=C1CC3=C4C=CC=CC4=CC=C3[O-]

InChI

InChIKey=SFOGBNDUKZYDID-UHFFFAOYSA-M
InChI=1S/C21H16O2.Na/c22-20-11-9-14-5-1-3-7-16(14)18(20)13-19-17-8-4-2-6-15(17)10-12-21(19)23;/h1-12,22-23H,13H2;/q;+1/p-1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
ST1859 reduces prion infectivity and increase survival in experimental scrapie.
2009
A positron emission tomography microdosing study with a potential antiamyloid drug in healthy volunteers and patients with Alzheimer's disease.
2006-09
Patents

Patents

Name Type Language
MONOSODIUM SQUOXINATE
Common Name English
2-NAPHTHALENOL, 1,1'-METHYLENEBIS-, MONOSODIUM SALT
Preferred Name English
MONOSODIUM 1,1'-METHYLENEBIS(2-NAPHTHOL)
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 57102
Created by admin on Mon Mar 31 21:50:20 GMT 2025 , Edited by admin on Mon Mar 31 21:50:20 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID20895778
Created by admin on Mon Mar 31 21:50:20 GMT 2025 , Edited by admin on Mon Mar 31 21:50:20 GMT 2025
PRIMARY
PUBCHEM
86278179
Created by admin on Mon Mar 31 21:50:20 GMT 2025 , Edited by admin on Mon Mar 31 21:50:20 GMT 2025
PRIMARY
CAS
38827-66-6
Created by admin on Mon Mar 31 21:50:20 GMT 2025 , Edited by admin on Mon Mar 31 21:50:20 GMT 2025
PRIMARY
FDA UNII
T8R9TK9A1Y
Created by admin on Mon Mar 31 21:50:20 GMT 2025 , Edited by admin on Mon Mar 31 21:50:20 GMT 2025
PRIMARY