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Details

Stereochemistry ACHIRAL
Molecular Formula C16H13Cl2NO4
Molecular Weight 354.185
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACECLOFENAC

SMILES

OC(=O)COC(=O)CC1=C(NC2=C(Cl)C=CC=C2Cl)C=CC=C1

InChI

InChIKey=MNIPYSSQXLZQLJ-UHFFFAOYSA-N
InChI=1S/C16H13Cl2NO4/c17-11-5-3-6-12(18)16(11)19-13-7-2-1-4-10(13)8-15(22)23-9-14(20)21/h1-7,19H,8-9H2,(H,20,21)

HIDE SMILES / InChI

Molecular Formula C16H13Cl2NO4
Molecular Weight 354.185
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:47:37 UTC 2023
Edited
by admin
on Fri Dec 15 15:47:37 UTC 2023
Record UNII
RPK779R03H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACECLOFENAC
EP   INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
ACECLOFENAC [EP MONOGRAPH]
Common Name English
Aceclofenac betadex [WHO-DD]
Common Name English
ACECLOFENAC [MART.]
Common Name English
GLYCOLIC ACID, (O-(2,6-DICHLOROANILINO)PHENYL)ACETATE (ESTER)
Common Name English
Aceclofenac [WHO-DD]
Common Name English
ACECLOFENAC [MI]
Common Name English
aceclofenac [INN]
Common Name English
ACECLOFENAC [JAN]
Common Name English
Classification Tree Code System Code
WHO-VATC QM02AA25
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
WHO-ATC M02AA25
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
WHO-VATC QM01AB16
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
WHO-ATC M01AB16
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
NCI_THESAURUS C257
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C80534
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
MERCK INDEX
m1293
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY Merck Index
FDA UNII
RPK779R03H
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
SMS_ID
100000092759
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
PUBCHEM
71771
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
RXCUI
16689
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY RxNorm
DRUG CENTRAL
43
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
WIKIPEDIA
ACECLOFENAC
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
INN
5608
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
DAILYMED
RPK779R03H
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
ChEMBL
CHEMBL93645
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
CAS
89796-99-6
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
EVMPD
SUB05200MIG
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
EPA CompTox
DTXSID7045522
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
MESH
C056498
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
CHEBI
31159
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
DRUG BANK
DB06736
Created by admin on Fri Dec 15 15:47:37 UTC 2023 , Edited by admin on Fri Dec 15 15:47:37 UTC 2023
PRIMARY
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