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
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)
| 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.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 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
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8580279
Single doses 0.1, 0.3 or 0.5 mg/kg
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:07:58 GMT 2025
by
admin
on
Mon Mar 31 18:07:58 GMT 2025
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| Record UNII |
C2R0GEU722
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C267
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C66885
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DTXSID70148049
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C2R0GEU722
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65900
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CHEMBL2106767
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107429-63-0
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C66018
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SUB08526MIG
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6788
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C065607
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100000082339
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ACTIVE MOIETY |