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Details

Stereochemistry ACHIRAL
Molecular Formula C14H19ClN4O2
Molecular Weight 310.779
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LINTOPRIDE

SMILES

CCN1CCN=C1CNC(=O)C2=CC(Cl)=C(N)C=C2OC

InChI

InChIKey=MJCKISCWHDATBN-UHFFFAOYSA-N
InChI=1S/C14H19ClN4O2/c1-3-19-5-4-17-13(19)8-18-14(20)9-6-10(15)11(16)7-12(9)21-2/h6-7H,3-5,8,16H2,1-2H3,(H,18,20)

HIDE SMILES / InChI

Molecular Formula C14H19ClN4O2
Molecular Weight 310.779
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Lintopride is a benzamide, eliciting prokinetic properties on the upper gut in several animal models. Lintopride increases gastric emptying, stimulates antral and duodenal motility and accelerates intestinal transit in animals. In canines it also increases lower oesophageal sphincter (LOS) pressure and reinforces peristaltic waves after wet swallowing, indicating a stimulatory action which could potentially be greater than that of metoclopramide. The 5HT-4 agonist lintopride increases LOS basal pressure and the amplitude of peristaltic waves of the oesophagus following a single intravenous dose in healthy subjects. The action of lintopride on LOS basal pressure and oesophageal peristaltic waves could be beneficial in patients with gastro-oesophageal reflux disease.

Approval Year

PubMed

PubMed

TitleDatePubMed
Post-synaptic 5-HT4 receptor modulation of tachykinergic excitation of rat oesophageal tunica muscularis mucosae.
1997-04-04
The effects of lintopride, a 5HT-4 antagonist, on oesophageal motility.
1995-10
High-performance liquid chromatographic determination of 4-amino-5-chloro-N-[(1-ethylimidazolin-2-yl)methyl]-2-methoxybenzamide and its metabolite in biological fluids. Applications in pharmacokinetic studies.
1990-06
Patents

Patents

Sample Use Guides

Single doses 0.1, 0.3 or 0.5 mg/kg
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:07:58 GMT 2025
Edited
by admin
on Mon Mar 31 18:07:58 GMT 2025
Record UNII
C2R0GEU722
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-AMINO-5-CHLORO-N-((1-ETHYL-2-IMIDAZOLIN-2-YL)METHYL)-O-ANISAMIDE
Preferred Name English
LINTOPRIDE
INN  
INN  
Official Name English
lintopride [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C267
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
NCI_THESAURUS C66885
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID70148049
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
FDA UNII
C2R0GEU722
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
PUBCHEM
65900
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106767
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
CAS
107429-63-0
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
NCI_THESAURUS
C66018
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
EVMPD
SUB08526MIG
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
INN
6788
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
MESH
C065607
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
SMS_ID
100000082339
Created by admin on Mon Mar 31 18:07:58 GMT 2025 , Edited by admin on Mon Mar 31 18:07:58 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY