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
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 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 |
| Name | Type | Language | ||
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
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DTXSID40957882
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23681574
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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
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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
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SUBSTANCE RECORD
