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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H32ClN3O4.ClH.H2O
Molecular Weight 480.426
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of REVEXEPRIDE MONOHYDROCHLORIDE MONOHYDRATE

SMILES

O.Cl.COCCCN1CC[C@@H](CNC(=O)C2=C3OC(C)(C)CC3=C(N)C(Cl)=C2)[C@H](O)C1

InChI

InChIKey=PBUJIMKARWFIMP-YUANJJMISA-N
InChI=1S/C21H32ClN3O4.ClH.H2O/c1-21(2)10-15-18(23)16(22)9-14(19(15)29-21)20(27)24-11-13-5-7-25(12-17(13)26)6-4-8-28-3;;/h9,13,17,26H,4-8,10-12,23H2,1-3H3,(H,24,27);1H;1H2/t13-,17+;;/m0../s1

HIDE SMILES / InChI
Revexepride is a selective 5-hydroxytryptamine receptor 4 agonist and member of a class of prokinetic agents that stimulate gastric emptying. Revexepride is thought to stimulate the release of acetylcholine at the myenteric plexus, leading to increased gastrointestinal contractions. This drug has been evaluated for potential use in treatment of gastroesophageal reflux disease. Phase I studies in healthy volunteers have shown no serious adverse events after administration of revexepride. However, a phase II study reported respiratory, thoracic and mediastinal disorders and pulmonary hypertension in 1 patient (0.85%). Furthermore, a European clinical trial showed that four weeks of treatment did not improve symptoms or gastric emptying in patients with symptoms suggestive of gastroparesis compared to placebo.

Approval Year

Name Type Language
REVEXEPRIDE MONOHYDROCHLORIDE MONOHYDRATE
Preferred Name English
Code System Code Type Description
PUBCHEM
131633444
Created by admin on Mon Mar 31 21:12:49 GMT 2025 , Edited by admin on Mon Mar 31 21:12:49 GMT 2025
PRIMARY
FDA UNII
B0P5ZFB497
Created by admin on Mon Mar 31 21:12:49 GMT 2025 , Edited by admin on Mon Mar 31 21:12:49 GMT 2025
PRIMARY