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

Details

Stereochemistry ACHIRAL
Molecular Formula C9H11NO2
Molecular Weight 165.1891
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHENZAMIDE

SMILES

CCOC1=CC=CC=C1C(N)=O

InChI

InChIKey=SBNKFTQSBPKMBZ-UHFFFAOYSA-N
InChI=1S/C9H11NO2/c1-2-12-8-6-4-3-5-7(8)9(10)11/h3-6H,2H2,1H3,(H2,10,11)

HIDE SMILES / InChI
Ethenzamide is an anti-inflammatory agent that was used for the treatment of common cold in Japan (in combinations with other NSAIDs).

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
NARON ACE

Approved Use

Unknown
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
100%
ETHENZAMIDE unknown
Homo sapiens
Doses

Doses

DosePopulationAdverse events​
500 mg single, oral
Studied dose
Dose: 500 mg
Route: oral
Route: single
Dose: 500 mg
Sources:
unhealthy
Health Status: unhealthy
Sex: F
Food Status: UNKNOWN
Sources:
Other AEs: Eruption...
Other AEs:
Eruption (1 pt)
Sources:
AEs

AEs

AESignificanceDosePopulation
Eruption 1 pt
500 mg single, oral
Studied dose
Dose: 500 mg
Route: oral
Route: single
Dose: 500 mg
Sources:
unhealthy
Health Status: unhealthy
Sex: F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Development, characterization and solubility study of solid dispersions of Cefuroxime Axetil by the solvent evaporation method.
2010-07
Drug-target interaction prediction from chemical, genomic and pharmacological data in an integrated framework.
2010-06-15
Ethenzamide-gentisic acid-acetic acid (2/1/1).
2010-04-10
Development, characterization and solubility study of solid dispersions of azithromycin dihydrate by solvent evaporation method.
2010-04
(13)C Solid-state NMR chromatography by magic angle spinning (1)H T(1) relaxation ordered spectroscopy.
2010-02
Development of theophylline floating microballoons using cellulose acetate butyrate and/or Eudragit RL 100 polymers with different permeability characteristics.
2010-01
Herringbone array of hydrogen-bonded ribbons in 2-ethoxybenzamide from high-resolution X-ray powder diffraction.
2009-11
Photodegradation of pharmaceuticals and personal care products during UV and UV/H2O2 treatments.
2009-10
Theophylline-gentisic acid (1/1).
2009-08-08
Distribution of ethenzamide and other ingredients on granule surfaces studied by Raman microspectroscopy and mapping.
2009-05
Assessing drug distribution in tissues expressing P-glycoprotein through physiologically based pharmacokinetic modeling: model structure and parameters determination.
2009-01-15
Evaluation of pharmaceuticals and personal care products as water-soluble molecular markers of sewage.
2008-09-01
One-step preparation of drug-containing microparticles to enhance the dissolution and absorption of poorly water-soluble drugs using a 4-fluid nozzle spray drier.
2007-07-31
Batch grinding kinetics of Ethenzamide particles by fluidized-bed jet-milling.
2006-03-27
Evaluation of rapidly disintegrating tablets containing glycine and carboxymethylcellulose.
2006-03-09
Dissolution characteristics of cylindrical particles and tablets.
2006-03-09
Continuous grinding kinetics of ethenzamide particles by fluidized-bed jet-milling.
2006-03
Influences of drugs on the oxygen uptake rate and biosorption of activated sludge.
2006-01
Variation in particle shape of active pharmaceutical ingredients prepared by fluidized-bed jet-milling.
2005-12
Effect of particle shape of active pharmaceutical ingredients prepared by fluidized-bed jet-milling on cohesiveness.
2005-05
Simultaneous determination of ingredients in a cold medicine by cyclodextrin-modified microemulsion electrokinetic chromatography.
2005-03-09
Salicylic acid-induced inactivation of creatine kinase in the presence of lactoperoxidase and H2O2.
2005-01-15
Grinding-induced equimolar complex formation between thiourea and ethenzamide.
2004-05
In vitro evaluation of floating and drug releasing behaviors of hollow microspheres (microballoons) prepared by the emulsion solvent diffusion method.
2004-03
Assessment of tableting properties using infinitesimal quantities of powdered medicine.
2003-09-16
Cutaneous drug reaction case reports: from the world literature.
2003
Preparation of solid dispersion for ethenzamide-carbopol and theophylline-carbopol systems using a twin screw extruder.
2002-06
Prediction of pharmacokinetics prior to in vivo studies. II. Generic physiologically based pharmacokinetic models of drug disposition.
2002-05
Preparation and clinical application of 2% diflunisal oral ointment for painful lesions of the oral mucosa.
2001-11
Determination of plasma bromvalerylurea and its main metabolite by a simple high-performance liquid chromatographic method and quantitation of bromide by energy dispersive X-ray spectrometry in carbon tetrachloride-intoxicated rats.
2001-08-15
Modifying effects of a mixture of acetaminophen, aspirin, dipyrone and ethenzamide on a multiorgan initiation model and its carcinogenicity in male F344 rats.
1999-01-08
Patents

Sample Use Guides

2 pills containing 84 mg of ethenzamide 3 times a day.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
ETHENZAMIDE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
J3.352I
Preferred Name English
Ethenzamide [WHO-DD]
Common Name English
ETHENZAMIDE [MI]
Common Name English
ETHENZAMIDE [JAN]
Common Name English
O-ETHOXYBENZAMIDE
Common Name English
ETENZAMIDE
Common Name English
NSC-28787
Code English
ethenzamide [INN]
Common Name English
ETHOXYBENZAMIDE
Systematic Name English
ETHENZAMIDE [MART.]
Common Name English
Classification Tree Code System Code
WHO-ATC N02BA77
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
NCI_THESAURUS C257
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
WHO-VATC QN02BA57
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
WHO-VATC QN02BA07
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
WHO-ATC N02BA07
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
WHO-ATC N02BA57
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
213-346-4
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
SMS_ID
100000082616
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
ChEMBL
CHEMBL1483877
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
EVMPD
SUB07274MIG
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
FDA UNII
L929ZCK4BF
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
EPA CompTox
DTXSID4020581
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
CAS
938-73-8
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
DRUG BANK
DB13544
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
MESH
C018935
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
PUBCHEM
3282
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
DRUG CENTRAL
1080
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
WIKIPEDIA
ETHENZAMIDE
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
NCI_THESAURUS
C87323
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
RXCUI
24468
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY RxNorm
INN
903
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
MERCK INDEX
m5056
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY Merck Index
NSC
28787
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY
DAILYMED
L929ZCK4BF
Created by admin on Mon Mar 31 21:24:10 GMT 2025 , Edited by admin on Mon Mar 31 21:24:10 GMT 2025
PRIMARY