| Name | 4-amino-5-chloro-N-[1-(3-methoxypropyl)piperidin-4-yl]-2,3-dihydro-1-benzofuran-7-carboxamide,hydrochloride |
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| Synonyms |
UNII-M8IYX9Z79V
Prucalopride hydrochloride |
| Description | Prucalopride hydrochloride is an orally active, selective and specific 5-HT4 receptor agonist (high affinity), with pKis of 8.6 and 8.1 for human 5-HT4a/4b receptors, respectively. Prucalopride hydrochloride improves intestinal motility by promoting regeneration of the intestinal nervous system in rats. Prucalopride hydrochloride also shows anticancer activity by blocking of the PI3K/AKT/mTor signaling pathway. Prucalopride hydrochloride can be used in studies of chronic constipation, pseudo-intestinal obstruction and cancer[1][2][3]. |
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| Related Catalog | |
| References |
| Molecular Formula | C18H27Cl2N3O3 |
|---|---|
| Molecular Weight | 404.33100 |
| Exact Mass | 403.14300 |
| PSA | 80.31000 |
| LogP | 3.98370 |