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Details

Stereochemistry ACHIRAL
Molecular Formula C15H15NO2
Molecular Weight 241.2851
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ENFENAMIC ACID

SMILES

OC(=O)C1=C(NCCC2=CC=CC=C2)C=CC=C1

InChI

InChIKey=HLNLBEFKHHCAMV-UHFFFAOYSA-N
InChI=1S/C15H15NO2/c17-15(18)13-8-4-5-9-14(13)16-11-10-12-6-2-1-3-7-12/h1-9,16H,10-11H2,(H,17,18)

HIDE SMILES / InChI
Enfenamic acid (under brand name tromaril) is an anthranilic acid derivative with potent anti-inflammatory, anti-arthritic, analgesic and antipyretic actions. It has additional unique property of anti-platelet aggregation activity, without disturbing any other blood coagulation factors. It also differs from other non-steroidal anti-inflammatory agents like indomethacin, in producing diuresis and natriuresis. In the clinical study, tromaril showed itself as a strong and effective drug for use in various eye diseases.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
Tromaril

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

Unknown
Route of Administration: Oral
In Vitro Use Guide
Incubation of liver cells in the presence of 1.0 mM enfenamic acid inhibited the output of glucose. And also the in vitro addition of various concentrations of enfenamic acid (0.25 to 3.0 mM) to the tissue extracts of liver inhibited the activities of important gluconeogenic enzymes such as pyruvate carboxylase (PC), phosphoenolpyruvate carboxykinase (PEPCK) and fructose 1,6-diphosphatase (FDPase). These findings indicated that the impairment of gluconeogenesis might be due to the inactivation of the enzymes by the drug.
Name Type Language
ENFENAMIC ACID
INN   MI   WHO-DD  
INN  
Official Name English
ENFENAMIC ACID [MI]
Common Name English
enfenamic acid [INN]
Common Name English
Enfenamic acid [WHO-DD]
Common Name English
N-PHENETHYLANTHRANILIC ACID
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
Code System Code Type Description
PUBCHEM
31635
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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EPA CompTox
DTXSID8057693
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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CAS
23049-93-6
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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MERCK INDEX
m1133
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
PRIMARY Merck Index
ChEMBL
CHEMBL2106178
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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SMS_ID
100000080229
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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EVMPD
SUB06529MIG
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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INN
4973
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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NCI_THESAURUS
C72088
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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MESH
C019126
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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FDA UNII
05KO5G76R2
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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DRUG CENTRAL
3176
Created by admin on Fri Dec 15 16:30:21 GMT 2023 , Edited by admin on Fri Dec 15 16:30:21 GMT 2023
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