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Details

Stereochemistry ACHIRAL
Molecular Formula C14H22BrN3O2.ClH
Molecular Weight 380.708
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BROMOPRIDE HYDROCHLORIDE

SMILES

Cl.CCN(CC)CCNC(=O)C1=CC(Br)=C(N)C=C1OC

InChI

InChIKey=SGQFXUUDHWNAIN-UHFFFAOYSA-N
InChI=1S/C14H22BrN3O2.ClH/c1-4-18(5-2)7-6-17-14(19)10-8-11(15)12(16)9-13(10)20-3;/h8-9H,4-7,16H2,1-3H3,(H,17,19);1H

HIDE SMILES / InChI

Molecular Formula C14H22BrN3O2
Molecular Weight 344.247
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Bromopride is a dopamine D2 receptor blocker. Bromopride exerts is a gastrointestinal prokinetic exploited clinically for the management of motor disorders of the upper gastrointestinal tract, including functional dyspepsia, gastric stasis of various origins and emesis.

CNS Activity

Originator

Curator's Comment: reference retrieved from www.drugfuture.com/chemdata/bromopride.html

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Bromopan

Approved Use

Principais: distúrbios digestivos psicossomáticos ad senectude e da estafa mental. Discinesias gastroduodenais e biliares. Colopatias espasmódicas. Enxaquecas e mal-estar de origem celíaca. Náuseas. Vômitos. Anorexia. Particulares: exames radiológicos do tubo digestivo. Preparação de explorações endoscópicas. Vômitos anestésicos. Soluços. Meteorismo abdominal pós-operatório. Manifestações digestivas após a aplicação de radioterapia.
PubMed

PubMed

TitleDatePubMed
Mirtazapine (Remeron) as treatment for non-mechanical vomiting after gastric bypass.
2005 May
Influence of bromopride in the prophylaxis of nausea associated with fluorescein angiography.
2007 Jan-Feb
Case-crossover study of Burkholderia cepacia complex bloodstream infection associated with contaminated intravenous bromopride.
2010 May
Patents

Patents

Sample Use Guides

Capsules: 40-60 mg/day Oral solution: 40-60 mg/day (adults), 0.5-1 mg/kg (children)
Route of Administration: Oral
In Vitro Use Guide
Bromopride effects on cholinesterase activity in plasma, striatum, duodenum and ileum of adult male rats were measured for drug concentrations ranging from 0.006 to 3.134 microM. Bromopride can inhibit cholinesterase activity in all tissues studied,
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:56:16 UTC 2023
Edited
by admin
on Fri Dec 15 17:56:16 UTC 2023
Record UNII
B7C7WX94Z6
Record Status Validated (UNII)
Record Version
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Name Type Language
BROMOPRIDE HYDROCHLORIDE
MI   WHO-DD  
Common Name English
BROMOPRIDE HYDROCHLORIDE [MI]
Common Name English
Bromopride hydrochloride [WHO-DD]
Common Name English
BENZAMIDE, 4-AMINO-5-BROMO-N-(2-(DIETHYLAMINO)ETHYL)-2-METHOXY-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
SMS_ID
100000089001
Created by admin on Fri Dec 15 17:56:16 UTC 2023 , Edited by admin on Fri Dec 15 17:56:16 UTC 2023
PRIMARY
MERCK INDEX
m2713
Created by admin on Fri Dec 15 17:56:16 UTC 2023 , Edited by admin on Fri Dec 15 17:56:16 UTC 2023
PRIMARY Merck Index
CAS
52423-56-0
Created by admin on Fri Dec 15 17:56:16 UTC 2023 , Edited by admin on Fri Dec 15 17:56:16 UTC 2023
PRIMARY
ECHA (EC/EINECS)
257-906-6
Created by admin on Fri Dec 15 17:56:16 UTC 2023 , Edited by admin on Fri Dec 15 17:56:16 UTC 2023
PRIMARY
PUBCHEM
3016754
Created by admin on Fri Dec 15 17:56:16 UTC 2023 , Edited by admin on Fri Dec 15 17:56:16 UTC 2023
PRIMARY
EVMPD
SUB23559
Created by admin on Fri Dec 15 17:56:16 UTC 2023 , Edited by admin on Fri Dec 15 17:56:16 UTC 2023
PRIMARY
MESH
C013855
Created by admin on Fri Dec 15 17:56:16 UTC 2023 , Edited by admin on Fri Dec 15 17:56:16 UTC 2023
PRIMARY
FDA UNII
B7C7WX94Z6
Created by admin on Fri Dec 15 17:56:16 UTC 2023 , Edited by admin on Fri Dec 15 17:56:16 UTC 2023
PRIMARY
EPA CompTox
DTXSID50966849
Created by admin on Fri Dec 15 17:56:16 UTC 2023 , Edited by admin on Fri Dec 15 17:56:16 UTC 2023
PRIMARY
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ACTIVE MOIETY