Prucalopride Succinate
Prucalopride succinate is the succinate salt form of prucalopride, a selective 5-HT4 receptor agonist that stimulates colonic peristalsis and gastrointestinal motility for the treatment of chronic idiopathic constipation. See prucalopride for complete pharmacological details.
分子量
486.0000 g/mol
TPSA
151.00 Ų
治療領域
作用機序
Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.
2D構造
Cite this structure
Embed this structure
SMILES
COCCCN1CCC(NC(=O)c2cc(Cl)c(N)c3c2OCC3)CC1.O=C(O)CCC(=O)O
InChI
InChI=1S/C18H26ClN3O3.C4H6O4/c1-24-9-2-6-22-7-3-12(4-8-22)21-18(23)14-11-15(19)16(20)13-5-10-25-17(13)14;5-3(6)1-2-4(7)8/h11-12H,2-10,20H2,1H3,(H,21,23);1-2H2,(H,5,6)(H,7,8)
Molecular Formula
C22H32ClN3O7
HBD / HBA
4 / 9
回転可能結合数
9
重原子数
33
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
よくある質問
Prucalopride succinate is the succinate salt form of prucalopride, a selective 5-HT4 receptor agonist that stimulates colonic peristalsis and gastrointestinal motility for the treatment of chronic idiopathic constipation. See prucalopride for complete pharmacological details.
Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.
Yes, Prucalopride Succinate is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2105748. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 9870009. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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