BUMADIZONE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Possibly Marketed Outside US

Details

Stereochemistry	RACEMIC
Molecular Formula	C19H22N2O3
Molecular Weight	326.3896
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BUMADIZONE

Structure Search

SMILES

CCCCC(C(O)=O)C(=O)N(NC1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=FLWFHHFTIRLFPV-UHFFFAOYSA-N

InChI=1S/C19H22N2O3/c1-2-3-14-17(19(23)24)18(22)21(16-12-8-5-9-13-16)20-15-10-6-4-7-11-15/h4-13,17,20H,2-3,14H2,1H3,(H,23,24)

HIDE SMILES / InChI

Molecular Formula	C19H22N2O3
Molecular Weight	326.3896
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Description
Sources: https://www.drugs.com/international/bumadizone.html | https://www.ncbi.nlm.nih.gov/pubmed/331502

Bumadizone is a non-steroidal anti-inflammatory drug exerting analgesic, antipyretic and anti-inflammatory properties. It has been studied in the treatment of rheumatoid diseases.

Approval Year

Patents

Patents

Sample Use Guides

In Vivo Use Guide

110 mg twice daily

Route of Administration: Oral

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:25:32 GMT 2025` Edited by `admin` on `Mon Mar 31 18:25:32 GMT 2025`
Record UNII	ATD81G944M
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

BUMADIZONE

Official Name

English

BUMADIZONE [MI]

Preferred Name

English

PHENYLBUTAZONE IMPURITY A [EP IMPURITY]

Common Name

English

BUTYLMALONIC ACID N,N'-DIPHENYLMONOHYDRAZIDE

Common Name

English

bumadizone [INN]

Common Name

English

Bumadizone [WHO-DD]

Common Name

English

Classification Tree Code System Code

WHO-ATC

M01AB07

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

NCI_THESAURUS

C257

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

WHO-VATC

QM01AB07

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

Code System Code Type Description

EVMPD

SUB05968MIG

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

WIKIPEDIA

Bumadizone

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

FDA UNII

ATD81G944M

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

EPA CompTox

DTXSID0022698

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

DRUG BANK

DB13286

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

ECHA (EC/EINECS)

222-710-1

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

INN

2847

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

CAS

3583-64-0

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

MESH

C100233

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

NCI_THESAURUS

C72113

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

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MERCK INDEX

m2758

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

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Merck Index

CHEBI

76119

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

SMS_ID

100000088459

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

RXCUI

19847

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

RxNorm

DRUG CENTRAL

426

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

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PUBCHEM

19161

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

ChEMBL

CHEMBL2105456

Created by admin on Mon Mar 31 18:25:32 GMT 2025 , Edited by admin on Mon Mar 31 18:25:32 GMT 2025

PRIMARY

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BUMADIZONE CALCIUM ANHYDROUS

SALT/SOLVATE -> PARENT


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BUMADIZONE CALCIUM

SALT/SOLVATE -> PARENT


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BUMADIZONE, (R)-

ENANTIOMER -> RACEMATE


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BUMADIZONE SODIUM

SALT/SOLVATE -> PARENT


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BUMADIZONE, (S)-

ENANTIOMER -> RACEMATE

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PARENT -> IMPURITY

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					ATD81G944M

ACTIVE MOIETY