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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
Structure of 5-HYDROXYDICLOFENAC

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)

HIDE SMILES / InChI

Molecular Formula C14H11Cl2NO3
Molecular Weight 312.148
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Human NAD(P)H:quinone oxidoreductase 1 (NQO1)-mediated inactivation of reactive quinoneimine metabolites of diclofenac and mefenamic acid.
2014-04-21
One-electron oxidation of diclofenac by human cytochrome P450s as a potential bioactivation mechanism for formation of 2'-(glutathion-S-yl)-deschloro-diclofenac.
2014-01-25
Diclofenac hypersensitivity: antibody responses to the parent drug and relevant metabolites.
2010-10-28
Removal of diclofenac and mefenamic acid by the white rot fungus Phanerochaete sordida YK-624 and identification of their metabolites after fungal transformation.
2010-09
Diclofenac oxidation by biogenic manganese oxides.
2010-05-01
Degradation of the drug sodium diclofenac by Trametes versicolor pellets and identification of some intermediates by NMR.
2010-04-15
Hepatic clearance of reactive glucuronide metabolites of diclofenac in the mouse is dependent on multiple ATP-binding cassette efflux transporters.
2010-04
Occurrence of diclofenac and its metabolites in surface water and effluent samples from Karachi, Pakistan.
2009-10
Occurrence of diclofenac and selected metabolites in sewage effluents.
2008-11-01
Oxidation of diclofenac with ozone in aqueous solution.
2008-09-01
Transformation of diclofenac by the indigenous microflora of river sediments and identification of a major intermediate.
2007-09
Investigation of the immunogenicity of diclofenac and diclofenac metabolites.
2007-01-10
Efficient high performance liquid chromatograph/ultraviolet method for determination of diclofenac and 4'-hydroxydiclofenac in rat serum.
2006-01-18
Effects of phenobarbital on metabolism and toxicity of diclofenac sodium in rat hepatocytes in vitro.
2004-10
Diclofenac-induced antibodies against red blood cells are heterogeneous and recognize different epitopes.
2004-08
Diclofenac and metabolite pharmacokinetics in children.
2004-06
Residue analysis of the pharmaceutical diclofenac in different water types using ELISA and GC-MS.
2003-08-01
Diclofenac-induced inactivation of CYP3A4 and its stimulation by quinidine.
2002-10
Mechanism-based inactivation of CYP2C11 by diclofenac.
2001-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:20:13 GMT 2025
Edited
by admin
on Mon Mar 31 19:20:13 GMT 2025
Record UNII
GS38436703
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5-HYDROXYDICLOFENAC
Common Name English
BENZENEACETIC ACID, 2-((2,6-DICHLOROPHENYL)AMINO)-5-HYDROXY-
Preferred Name English
HYDROXYDICLOFENAC, 5-
Common Name English
Code System Code Type Description
PUBCHEM
3052566
Created by admin on Mon Mar 31 19:20:13 GMT 2025 , Edited by admin on Mon Mar 31 19:20:13 GMT 2025
PRIMARY
CAS
69002-84-2
Created by admin on Mon Mar 31 19:20:13 GMT 2025 , Edited by admin on Mon Mar 31 19:20:13 GMT 2025
PRIMARY
FDA UNII
GS38436703
Created by admin on Mon Mar 31 19:20:13 GMT 2025 , Edited by admin on Mon Mar 31 19:20:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID00219059
Created by admin on Mon Mar 31 19:20:13 GMT 2025 , Edited by admin on Mon Mar 31 19:20:13 GMT 2025
PRIMARY
Related Record Type Details
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