U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C14H11Cl2NO2
Molecular Weight 296.149
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MECLOFENAMIC ACID

SMILES

CC1=CC=C(Cl)C(NC2=C(C=CC=C2)C(O)=O)=C1Cl

InChI

InChIKey=SBDNJUWAMKYJOX-UHFFFAOYSA-N
InChI=1S/C14H11Cl2NO2/c1-8-6-7-10(15)13(12(8)16)17-11-5-3-2-4-9(11)14(18)19/h2-7,17H,1H3,(H,18,19)

HIDE SMILES / InChI

Molecular Formula C14H11Cl2NO2
Molecular Weight 296.149
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 Sat Dec 16 17:19:21 UTC 2023
Edited
by admin
on Sat Dec 16 17:19:21 UTC 2023
Record UNII
48I5LU4ZWD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MECLOFENAMIC ACID
GREEN BOOK   INN   MART.   MI   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
CL-583
Code English
BENZOIC ACID, 2-((2,6-DICHLORO-3-METHYLPHENYL)AMINO)-
Common Name English
N-(2,6-DICHLORO-M-TOLYL)ANTHRANILIC ACID
Systematic Name English
MECLOFENAMATE
VANDF  
Common Name English
Meclofenamic acid [WHO-DD]
Common Name English
MECLOFENAMIC ACID [MART.]
Common Name English
meclofenamic acid [INN]
Common Name English
INF 4668
Code English
MECLOFENAMATE [VANDF]
Common Name English
NSC-95309
Code English
INF-4668
Code English
MECLOFENAMIC ACID [VANDF]
Common Name English
MECLOFENAMIC ACID [MI]
Common Name English
CI-583
Code English
MECLOFENAMIC ACID [USAN]
Common Name English
MECLOFENAMIC ACID [GREEN BOOK]
Common Name English
Classification Tree Code System Code
LIVERTOX 588
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
WHO-ATC M01AG04
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
WHO-VATC QM01AG04
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
NCI_THESAURUS C1323
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
CFR 21 CFR 520.1330
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
WHO-VATC QM02AA18
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
WHO-ATC M02AA18
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
CFR 21 CFR 520.1331
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
Code System Code Type Description
FDA UNII
48I5LU4ZWD
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
MESH
D008469
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
SMS_ID
100000081757
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
DAILYMED
48I5LU4ZWD
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
MERCK INDEX
m7120
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY Merck Index
INN
2165
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
IUPHAR
7219
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
DRUG BANK
DB00939
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
NSC
95309
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
RXCUI
588003
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
ALTERNATIVE
CHEBI
76230
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
CAS
644-62-2
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
PUBCHEM
4037
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
LACTMED
Meclofenamate
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
NCI_THESAURUS
C61826
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
EVMPD
SUB08678MIG
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
EPA CompTox
DTXSID0048559
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
RXCUI
6678
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
ECHA (EC/EINECS)
211-419-5
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
CHEBI
6710
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
ChEMBL
CHEMBL509
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
DRUG CENTRAL
1650
Created by admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
PRIMARY
Related Record Type Details
METABOLIC ENZYME -> INHIBITOR
POTENT
SALT/SOLVATE -> PARENT
Related Record Type Details
METABOLITE ACTIVE -> PARENT
Urinary excretion accounts for up to 50-60% of this metabolites. (Active)
MAJOR
URINE
METABOLITE INACTIVE -> PARENT
Related Record Type Details
ACTIVE MOIETY