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
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
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 |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
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
Edited
Sat Dec 16 11:30:51 GMT 2023
by
admin
on
Sat Dec 16 11:30:51 GMT 2023
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Record UNII |
3L8J50YGSQ
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Record Status |
Validated (UNII)
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Record Version |
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23681574
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36616-53-2
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admin on Sat Dec 16 11:30:51 GMT 2023 , Edited by admin on Sat Dec 16 11:30:51 GMT 2023
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |