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Details

Stereochemistry RACEMIC
Molecular Formula 2C19H21N2O3.Ca
Molecular Weight 690.841
Optical Activity ( + / - )
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUMADIZONE CALCIUM ANHYDROUS

SMILES

[Ca++].CCCCC(C([O-])=O)C(=O)N(NC1=CC=CC=C1)C2=CC=CC=C2.CCCCC(C([O-])=O)C(=O)N(NC3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=RKINNRASCJRSHD-UHFFFAOYSA-L
InChI=1S/2C19H22N2O3.Ca/c2*1-2-3-14-17(19(23)24)18(22)21(16-12-8-5-9-13-16)20-15-10-6-4-7-11-15;/h2*4-13,17,20H,2-3,14H2,1H3,(H,23,24);/q;;+2/p-2

HIDE SMILES / InChI

Molecular Formula Ca
Molecular Weight 40.078
Charge 2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C19H21N2O3
Molecular Weight 325.3816
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

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 Fri Dec 15 17:16:19 GMT 2023
Edited
by admin
on Fri Dec 15 17:16:19 GMT 2023
Record UNII
142R7TU2TN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUMADIZONE CALCIUM ANHYDROUS
Common Name English
(±)-MALONIC ACID, BUTYL-, MONO(1,2-DIPHENYLHYDRAZIDE), CALCIUM SALT (2:1)
Common Name English
PROPANEDIOIC ACID, 2-BUTYL-, 1-(1,2-DIPHENYLHYDRAZIDE), CALCIUM SALT (2:1)
Common Name English
MALONIC ACID, BUTYL-, MONO(1,2-DIPHENYLHYDRAZIDE), CALCIUM SALT (2:1)
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID30956006
Created by admin on Fri Dec 15 17:16:19 GMT 2023 , Edited by admin on Fri Dec 15 17:16:19 GMT 2023
PRIMARY
PUBCHEM
36833
Created by admin on Fri Dec 15 17:16:19 GMT 2023 , Edited by admin on Fri Dec 15 17:16:19 GMT 2023
PRIMARY
CAS
34461-73-9
Created by admin on Fri Dec 15 17:16:19 GMT 2023 , Edited by admin on Fri Dec 15 17:16:19 GMT 2023
PRIMARY
ECHA (EC/EINECS)
252-048-9
Created by admin on Fri Dec 15 17:16:19 GMT 2023 , Edited by admin on Fri Dec 15 17:16:19 GMT 2023
PRIMARY
FDA UNII
142R7TU2TN
Created by admin on Fri Dec 15 17:16:19 GMT 2023 , Edited by admin on Fri Dec 15 17:16:19 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
SOLVATE->ANHYDROUS
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY