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

Details

Stereochemistry RACEMIC
Molecular Formula C19H26NO.Br
Molecular Weight 364.32
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BIBENZONIUM BROMIDE

SMILES

[Br-].C[N+](C)(C)CCOC(CC1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=APVMLVNTOWQOHL-UHFFFAOYSA-M
InChI=1S/C19H26NO.BrH/c1-20(2,3)14-15-21-19(18-12-8-5-9-13-18)16-17-10-6-4-7-11-17;/h4-13,19H,14-16H2,1-3H3;1H/q+1;/p-1

HIDE SMILES / InChI

Molecular Formula C19H26NO
Molecular Weight 284.4158
Charge 1
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula BrH
Molecular Weight 80.912
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Bibenzonium is an antitussive agent. Bibenzonium bromide is a cough suppressant which is stated to have a central action.

Approval Year

Sample Use Guides

30 mg two to three times daily
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:43:10 GMT 2023
Edited
by admin
on Fri Dec 15 15:43:10 GMT 2023
Record UNII
4455J9277Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BIBENZONIUM BROMIDE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
BIBENZONIUM BROMIDE [MART.]
Common Name English
BIBENZONIUM BROMIDE [MI]
Common Name English
bibenzonium bromide [INN]
Common Name English
Bibenzonium bromide [WHO-DD]
Common Name English
SODOBEX
Brand Name English
(2-(1,2-DIPHENYLETHOXY)ETHYLTRIMETHYL)AMMONIUM BROMIDE
Common Name English
Classification Tree Code System Code
WHO-VATC QR05DB12
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
NCI_THESAURUS C66917
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
WHO-ATC R05DB12
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2110796
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
CAS
15585-70-3
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
DRUG BANK
DBSALT002525
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
MERCK INDEX
m587
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID80875177
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
EVMPD
SUB05815MIG
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
FDA UNII
4455J9277Q
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
INN
1263
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
WIKIPEDIA
BIBENZONIUM BROMIDE
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
ECHA (EC/EINECS)
239-643-9
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
PUBCHEM
85001
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
NCI_THESAURUS
C73180
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
SMS_ID
100000085877
Created by admin on Fri Dec 15 15:43:10 GMT 2023 , Edited by admin on Fri Dec 15 15:43:10 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY