Prucaloprideisanorally-available,dibenzofuran-based,enterokineticagoNISTofthehumanSEROtonin5-HT4aand5-HT4breceptorisoformswithKiestimatesof3nMand8nM,respectively.IthasmodestselectivityoverthehumanD4receptor(2.3uM),mouse5-HT3receptor(3.7uM)andhumans1receptor(3.7uM).(1,2)
InitialtolerABIlitystudiesshowthatprucalopridedoesnotencountercardiotoxicityissuestotheextentseeninotherdrugsofthisclass.[3]
Technicalinformation:
ChemicalFormula: | C18H26ClN3O3 | |
CAS#: | 179474-81-8 | |
MolecularWeight: | 367.87 | |
Purity: >98% | ||
Appearance: | White | |
ChemicalName: | 7-Benzofurancarboxamide,4-amino-5-chloro-2,3-dihydro-N-[1-(3-methoxypropyl)-4-piperidinyl] | |
Solubility: | Upto100mMinDMSO | |
Synonyms: | 0 |
ShippingCondition:Theproductisshippedinaglassvialatambienttemperature.
Storagecondition:Forlongershelflife,storesolidpowderat4oCdesiccated,orstoreDMSOsolutionat-20oC.
Reference:
1. | Briejeretal.,Theinvitropharmacologicalprofileofprucalopride,anovelenterokineticcompound,Eur.J.Pharmcol.2001,423,71-83.PubmedID:11438309 |
2. | Framptonetal.,Prucalopride:ADISDrugProfile.Drugs,2009,69(17),2453-2476.PubmedID:19911858 |
3. | Quigleyetal.,Prucalopride:safety,efficacyandpotentialapplications.Ther.Adv.Gastroenterol.2012,5(1),23-30. |
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