Drugs Information:
Prucalopride
Basic Information
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ID | DDInter1544 | |
Drug Type | small molecule | |
Molecular Formula | C18H26ClN3O3 | |
Molecular Weight | 367.870 | |
CAS Number | 179474-81-8 | |
Description | Prucalopride is a dihydrobenzofurancarboxamide derivative from the benzofurane family that selectively stimulates 5-HT4 receptors and thus, it presents enterokinetic properties.[A37348] The high selectivity of prucalopride allowed further development as it prevented the cardiac adverse reactions observed due to non-target effects of precedent therapies.[A40254] Prucalopride was developed by Shire Development LLC and approved for use in Europe in 2009,[A40250] in Canada on December 7, 2011 and by the FDA on December 17, 2018.[L4880] | |
ATC Classification | A06AX05 | |
IUPAC Name | 4-amino-5-chloro-N-[1-(3-methoxypropyl)piperidin-4-yl]-2,3-dihydro-1-benzofuran-7-carboxamide | |
InChI | ZPMNHBXQOOVQJL-UHFFFAOYSA-N | |
Canonical SMILES | COCCCN1CCC(CC1)NC(=O)C1=C2OCCC2=C(N)C(Cl)=C1 | |
Useful Links | DrugBank ChEBI PubChem Substance ChemSpider BindingDB Wikipedia ChEMBL ZINC |
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Prucalopride
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