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Details

Stereochemistry RACEMIC
Molecular Formula C14H15Cl2O2.Na
Molecular Weight 309.163
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENCLORAC SODIUM

SMILES

[Na+].[O-]C(=O)C(Cl)C1=CC=C(C2CCCCC2)C(Cl)=C1

InChI

InChIKey=BIBPNOSOPLBYIZ-UHFFFAOYSA-M
InChI=1S/C14H16Cl2O2.Na/c15-12-8-10(13(16)14(17)18)6-7-11(12)9-4-2-1-3-5-9;/h6-9,13H,1-5H2,(H,17,18);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C14H15Cl2O2
Molecular Weight 286.174
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Fenclorac is a potent nonsteroidal anti-inflammatory agent with significant analgesic and antipyretic activity. It inhibits prostaglandin synthesis both in vitro and in vivo.

Approval Year

PubMed

PubMed

TitleDatePubMed
The inhibition of prostaglandin synthetase in vivo by nonsteroidal anti-inflammatory agents.
1977-07
Studies on the in vitro inhibition of prostaglandin synthetase by fenclorac (alpha, m-dichloro-p-cyclohexylphenylacetic acid) and indomethacin.
1977-06-01
The antiphlogistic, antinociceptive and antipyretic properties of fenclorac.
1976-11
Inhibition of the diarrheal and cardiac actions of arachidonic acid by fenclorac, a new anti-inflammatory agent.
1976-10-15
Substance Class Chemical
Created
by admin
on Tue Apr 01 16:29:36 GMT 2025
Edited
by admin
on Tue Apr 01 16:29:36 GMT 2025
Record UNII
3L8J50YGSQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENCLORAC SODIUM
Common Name English
.ALPHA.,M-DICHLORO-P-CYCLOHEXYLPHENYLACETIC ACID, SODIUM SALT
Preferred Name English
BENZENEACETIC ACID, .ALPHA.,3-DICHLORO-4-CYCLOHEXYL-, SODIUM SALT (1:1)
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID40957882
Created by admin on Tue Apr 01 16:29:36 GMT 2025 , Edited by admin on Tue Apr 01 16:29:36 GMT 2025
PRIMARY
PUBCHEM
23681574
Created by admin on Tue Apr 01 16:29:36 GMT 2025 , Edited by admin on Tue Apr 01 16:29:36 GMT 2025
PRIMARY
FDA UNII
3L8J50YGSQ
Created by admin on Tue Apr 01 16:29:36 GMT 2025 , Edited by admin on Tue Apr 01 16:29:36 GMT 2025
PRIMARY
CAS
36616-53-2
Created by admin on Tue Apr 01 16:29:36 GMT 2025 , Edited by admin on Tue Apr 01 16:29:36 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE