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

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 antiphlogistic, antinociceptive and antipyretic properties of fenclorac.
1976 Nov
Inhibition of the diarrheal and cardiac actions of arachidonic acid by fenclorac, a new anti-inflammatory agent.
1976 Oct 15
The inhibition of prostaglandin synthetase in vivo by nonsteroidal anti-inflammatory agents.
1977 Jul
Studies on the in vitro inhibition of prostaglandin synthetase by fenclorac (alpha, m-dichloro-p-cyclohexylphenylacetic acid) and indomethacin.
1977 Jun 1
Substance Class Chemical
Created
by admin
on Sat Dec 16 11:30:51 GMT 2023
Edited
by admin
on Sat Dec 16 11:30:51 GMT 2023
Record UNII
3L8J50YGSQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENCLORAC SODIUM
Common Name English
BENZENEACETIC ACID, .ALPHA.,3-DICHLORO-4-CYCLOHEXYL-, SODIUM SALT (1:1)
Systematic Name English
.ALPHA.,M-DICHLORO-P-CYCLOHEXYLPHENYLACETIC ACID, SODIUM SALT
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID40957882
Created by admin on Sat Dec 16 11:30:51 GMT 2023 , Edited by admin on Sat Dec 16 11:30:51 GMT 2023
PRIMARY
PUBCHEM
23681574
Created by admin on Sat Dec 16 11:30:51 GMT 2023 , Edited by admin on Sat Dec 16 11:30:51 GMT 2023
PRIMARY
FDA UNII
3L8J50YGSQ
Created by admin on Sat Dec 16 11:30:51 GMT 2023 , Edited by admin on Sat Dec 16 11:30:51 GMT 2023
PRIMARY
CAS
36616-53-2
Created by admin on Sat Dec 16 11:30:51 GMT 2023 , Edited by admin on Sat Dec 16 11:30:51 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE