Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H11Cl2NO3 |
| Molecular Weight | 312.148 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CC1=CC(O)=CC=C1NC2=C(Cl)C=CC=C2Cl
InChI
InChIKey=VNQURRWYKFZKJZ-UHFFFAOYSA-N
InChI=1S/C14H11Cl2NO3/c15-10-2-1-3-11(16)14(10)17-12-5-4-9(18)6-8(12)7-13(19)20/h1-6,17-18H,7H2,(H,19,20)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Mechanism-based inactivation of CYP2C11 by diclofenac. | 2001 Sep |
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| Residue analysis of the pharmaceutical diclofenac in different water types using ELISA and GC-MS. | 2003 Aug 1 |
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| Diclofenac-induced antibodies against red blood cells are heterogeneous and recognize different epitopes. | 2004 Aug |
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| Diclofenac and metabolite pharmacokinetics in children. | 2004 Jun |
|
| Diclofenac oxidation by biogenic manganese oxides. | 2010 May 1 |
|
| Diclofenac hypersensitivity: antibody responses to the parent drug and relevant metabolites. | 2010 Oct 28 |
|
| Removal of diclofenac and mefenamic acid by the white rot fungus Phanerochaete sordida YK-624 and identification of their metabolites after fungal transformation. | 2010 Sep |
|
| Human NAD(P)H:quinone oxidoreductase 1 (NQO1)-mediated inactivation of reactive quinoneimine metabolites of diclofenac and mefenamic acid. | 2014 Apr 21 |
|
| One-electron oxidation of diclofenac by human cytochrome P450s as a potential bioactivation mechanism for formation of 2'-(glutathion-S-yl)-deschloro-diclofenac. | 2014 Jan 25 |
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3052566
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69002-84-2
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GS38436703
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DTXSID00219059
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admin on Fri Dec 15 18:44:55 GMT 2023 , Edited by admin on Fri Dec 15 18:44:55 GMT 2023
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PARENT (METABOLITE)
SUBSTANCE RECORD
