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Details

Stereochemistry ACHIRAL
Molecular Formula C19H19NO6
Molecular Weight 357.3573
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETERSALATE

SMILES

CC(=O)NC1=CC=C(OCCOC(=O)C2=C(OC(C)=O)C=CC=C2)C=C1

InChI

InChIKey=PXBFSRVXEKCBFP-UHFFFAOYSA-N
InChI=1S/C19H19NO6/c1-13(21)20-15-7-9-16(10-8-15)24-11-12-25-19(23)17-5-3-4-6-18(17)26-14(2)22/h3-10H,11-12H2,1-2H3,(H,20,21)

HIDE SMILES / InChI

Molecular Formula C19H19NO6
Molecular Weight 357.3573
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Etersalate is a derivative of aspirin exerting antiplatelet, analgesic, anti-inflammatory and antipyretic properties. Etersalate has potential to prevent oligomerization of amyloid beta (Aβ) peptides.

Originator

Curator's Comment: reference retrieved from https://www.drugfuture.com/chemdata/etersalate.html

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Etersalate prevents the formations of 6Aβ16-22 oligomer: An in silico study.
2018
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:11:12 GMT 2023
Edited
by admin
on Sat Dec 16 17:11:12 GMT 2023
Record UNII
653GN04T2G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETERSALATE
INN   MART.   MI  
INN  
Official Name English
etersalate [INN]
Common Name English
ETERYLATE
WHO-DD  
Common Name English
Eterylate [WHO-DD]
Common Name English
ETERSALATE [MART.]
Common Name English
SALICYLIC ACID ACETATE, ESTER WITH .BETA.-HYDROXY-P-ACETOPHENETIDIDE
Common Name English
ETERSALATE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID60212203
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104226
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
EVMPD
SUB12448MIG
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
FDA UNII
653GN04T2G
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
SMS_ID
100000078753
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
ECHA (EC/EINECS)
263-780-3
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
DRUG CENTRAL
1070
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
CAS
62992-61-4
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
PUBCHEM
44258
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
MERCK INDEX
m170
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY Merck Index
INN
5378
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
NCI_THESAURUS
C65558
Created by admin on Sat Dec 16 17:11:12 GMT 2023 , Edited by admin on Sat Dec 16 17:11:12 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY